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Buy Azocine Cas 292-65-9

Buy Azocine Cas 292-65-9

Buy Azocine Cas 292-65-9

Azocine is a heterocyclic organic compound with the molecular formula C7H7N. It consists of an unsaturated eight-membered ring having seven carbon atoms, one nitrogen atom and four double bonds. Buy Azocine Cas 292-65-9

Saturated or partially saturated azocine rings form the core structure of a group of opioid compounds sometimes known as azocines. These include cyclazocinepentazocine, and phenazocine.

The fully saturated analog of azocine is azocane.

Azocine rings are found in many natural products, including the manzamine family of marine alkaloids. One such compound is nakadomarin A, which contains a partially saturated azocine within its hexacyclic fused ring system. Nakadomarin A has been investigated as a potential antibiotic. Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9, Buy Azocine Cas 292-65-9

Source and Classification

Azocine can be derived from various natural and synthetic sources. It is often found in alkaloids and opioids, such as cyclazocine and nakadomarin A, which are known for their pharmacological effects  . In terms of classification, azocine is categorized as a bicyclic compound due to its two fused rings, one of which is a nitrogen-containing heterocycle.

Synthesis Analysis

Methods and Technical Details

The synthesis of azocine has evolved significantly over the years, with several methods being developed:

  1. Ring-Expansion Reactions: This method involves embedding a fragment into an existing ring structure to form an eight-membered ring. It is one of the most common pathways for synthesizing azocines  .
  2. Intramolecular Heck Reaction: This reaction utilizes unsaturated halides or triflates in the presence of a catalyst to form substituted alkenes, facilitating the formation of azocines  .
  3. Cycloaddition Reactions: Notably, the Diels-Alder reaction has been adapted for azocine synthesis, allowing linear molecules to combine and form cyclic structures  .
  4. Ring-Closing Metathesis: This method involves the redistribution of substituents with double bonds to close an eight-membered ring. It was recognized with a Nobel Prize in Chemistry for its significance in organic synthesis  .
  5. Microwave-Assisted Reactions: These reactions enhance the efficiency of cyclization processes leading to azocine formation  .

Recent studies have also highlighted the use of cascade reactions and thermolysis as effective methods for synthesizing azocines   .

Molecular Structure Analysis

Structure and Data

The molecular structure of azocine consists of a saturated nitrogen atom within an eight-membered ring framework. The presence of four double bonds contributes to its unique chemical properties. The bond angles and lengths are crucial for understanding its reactivity and interactions with biological targets.

  • Molecular FormulaC7H7N
  • Molecular Weight: Approximately 119.14 g/mol
  • Structural Representation:
    Azocine Structure:

/ \ /
C C-C C
\ | /
C—C

Properties

CAS Number

292-65-9

Product Name

Azocine

IUPAC Name

(3Z,5Z,7Z)-azocine

Molecular Formula

C7H7N

Molecular Weight

105.14 g/mol

InChI

InChI=1S/C7H7N/c1-2-4-6-8-7-5-3-1/h1-7H/b2-1-,3-1?,4-2?,5-3-,6-4-,7-5?,8-6?,8-7?

InChI Key

XXRGLCKZBCIEKO-BCLLOLPUSA-N

Canonical SMILES

C1=CC=CN=CC=C1

Isomeric SMILES

C\1=C\C=C/N=C\C=C1
 

Identification

1.1GHS Product identifier

Product name azocine

1.2Other means of identification

Product number
Other names Azocin

1.3Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4Supplier’s details

Company
Address
Telephone
Fax

1.5Emergency phone number

Emergency phone number
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

2.Hazard identification

2.1Classification of the substance or mixture

no data available

2.2GHS label elements, including precautionary statements

Pictogram(s) no data available
Signal word no data available
Hazard statement(s) no data available
Precautionary statement(s)
Prevention no data available
Response no data available
Storage no data available
Disposal no data available

2.3Other hazards which do not result in classification

no data available

3.Composition/information on ingredients

3.1Substances

Chemical name Common names and synonyms CAS number EC number Concentration
azocine azocine 292-65-9 none 100%

4.First-aid measures

4.1Description of necessary first-aid measures

General advice

Consult a physician. Show this safety data sheet to the doctor in attendance.

If inhaled

If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician.

In case of skin contact

Wash off with soap and plenty of water. Consult a physician.

In case of eye contact

Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.

If swallowed

Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.

4.2Most important symptoms/effects, acute and delayed

no data available

4.3Indication of immediate medical attention and special treatment needed, if necessary

no data available

5.Fire-fighting measures

5.1Extinguishing media

Suitable extinguishing media

Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.

5.2Specific hazards arising from the chemical

no data available

5.3Special protective actions for fire-fighters

Wear self-contained breathing apparatus for firefighting if necessary.

6.Accidental release measures

6.1Personal precautions, protective equipment and emergency procedures

Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. For personal protection see section 8.

6.2Environmental precautions

Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided.

6.3Methods and materials for containment and cleaning up

Pick up and arrange disposal. Sweep up and shovel. Keep in suitable, closed containers for disposal.

7.Handling and storage

7.1Precautions for safe handling

Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Avoid exposure – obtain special instructions before use.Provide appropriate exhaust ventilation at places where dust is formed. For precautions see section 2.2.

7.2Conditions for safe storage, including any incompatibilities

Store in cool place. Keep container tightly closed in a dry and well-ventilated place.

8.Exposure controls/personal protection

8.1Control parameters

Occupational Exposure limit values

no data available

Biological limit values

no data available

8.2Appropriate engineering controls

Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday.

8.3Individual protection measures, such as personal protective equipment (PPE)

Eye/face protection

Safety glasses with side-shields conforming to EN166. Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection

Wear impervious clothing. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace. Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique(without touching glove’s outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it.

Respiratory protection

Wear dust mask when handling large quantities.

Thermal hazards

no data available

9.Physical and chemical properties

Physical state no data available
Colour no data available
Odour no data available
Melting point/ freezing point no data available
Boiling point or initial boiling point and boiling range no data available
Flammability no data available
Lower and upper explosion limit / flammability limit no data available
Flash point no data available
Auto-ignition temperature no data available
Decomposition temperature no data available
pH no data available
Kinematic viscosity no data available
Solubility no data available
Partition coefficient n-octanol/water (log value) no data available
Vapour pressure no data available
Density and/or relative density no data available
Relative vapour density no data available
Particle characteristics no data available

10.Stability and reactivity

10.1Reactivity

no data available

10.2Chemical stability

Stable under recommended storage conditions.

10.3Possibility of hazardous reactions

no data available

10.4Conditions to avoid

no data available

10.5Incompatible materials

no data available

10.6Hazardous decomposition products

no data available

11.Toxicological information

Acute toxicity

  • Oral: no data available
  • Inhalation: no data available
  • Dermal: no data available

Skin corrosion/irritation

no data available

Serious eye damage/irritation

no data available

Respiratory or skin sensitization

no data available

Germ cell mutagenicity

no data available

Carcinogenicity

no data available

Reproductive toxicity

no data available

STOT-single exposure

no data available

STOT-repeated exposure

no data available

Aspiration hazard

no data available

12.Ecological information

12.1Toxicity

  • Toxicity to fish: no data available
  • Toxicity to daphnia and other aquatic invertebrates: no data available
  • Toxicity to algae: no data available
  • Toxicity to microorganisms: no data available

12.2Persistence and degradability

no data available

12.3Bioaccumulative potential

no data available

12.4Mobility in soil

no data available

12.5Other adverse effects

no data available

13.Disposal considerations

13.1Disposal methods

Product

The material can be disposed of by removal to a licensed chemical destruction plant or by controlled incineration with flue gas scrubbing. Do not contaminate water, foodstuffs, feed or seed by storage or disposal. Do not discharge to sewer systems.

Contaminated packaging

Containers can be triply rinsed (or equivalent) and offered for recycling or reconditioning. Alternatively, the packaging can be punctured to make it unusable for other purposes and then be disposed of in a sanitary landfill. Controlled incineration with flue gas scrubbing is possible for combustible packaging materials.

14.Transport information

Azocine is a heterocyclic compound with a nine-membered ring structure, consisting of seven carbon atoms and two nitrogen atoms. It is an aromatic compound, similar to other azines, and is known for its unique chemical properties. Azocine derivatives have potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, due to their diverse reactivity and stability. The compound’s structure allows for the formation of various functional groups and substitution patterns, making it a versatile building block for the synthesis of complex molecules.

292-65-9

Post Buying Request

  • 292-65-9 Structure
  • Basic information

    1. Product Name: Azocine
    2. Synonyms: Azacyclooctatetraene;Azocine
    3. CAS NO:292-65-9
    4. Molecular Formula: C7H7 N
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 292-65-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 217.7°C at 760 mmHg
    3. Flash Point: 77°C
    4. Appearance: /
    5. Density: 0.86g/cm3
    6. Vapor Pressure: 0.193mmHg at 25°C
    7. Refractive Index: 1.495
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Azocine(CAS DataBase Reference)
    11. NIST Chemistry Reference: Azocine(292-65-9)
    12. EPA Substance Registry System: Azocine(292-65-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 292-65-9(Hazardous Substances Data)

292-65-9 Suppliers

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292-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 292-65-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 292-65:
(5*2)+(4*9)+(3*2)+(2*6)+(1*5)=69
69 % 10 = 9
So 292-65-9 is a valid CAS Registry Number.

InChI:InChI=1/C7H7N/c1-2-4-6-8-7-5-3-1/h1-7H/b2-1-,3-1-,4-2-,5-3-,6-4-,7-5-,8-6-,8-7-

292-65-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) – Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name azocine

1.2 Other means of identification

Product number
Other names Azocin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier’s details

1.5 Emergency phone number

Emergency phone number
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).
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