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Number: 93675-25-3
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Basic information
- Product Name: 3-MMA
- Synonyms: Benzeneethanamine, 3-methoxy-N,alpha-dimethyl-;1-(3-methoxyphenyl)-N-methyl-propan-2-amine;3-Methoxy-4-methylamphetamine;
- CAS NO:93675-25-3
- Molecular Formula: C11H17NO
- Molecular Weight: 179.262
- EINECS: N/A
- Product Categories: N/A
-
Chemical Properties
- Melting Point: N/A
- Boiling Point: 262.5°Cat760mmHg
- Flash Point: 106.5°C
- Appearance: N/A
- Density: 0.951g/cm3
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 3-MMA(CAS DataBase Reference)
- NIST Chemistry Reference: 3-MMA(93675-25-3)
- EPA Substance Registry System: 3-MMA(93675-25-3)
-
Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 93675-25-3(Hazardous Substances Data)
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Check Digit Verification of cas no
The CAS Registry Mumber 93675-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,7 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93675-25:
(7*9)+(6*3)+(5*6)+(4*7)+(3*5)+(2*2)+(1*5)=163
163 % 10 = 3
So 93675-25-3 is a valid CAS Registry Number.
93675-25-3SDS
SAFETY DATA SHEETS
According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) – Sixth revised edition
Version: 1.0
Creation Date: Aug 15, 2017
Revision Date: Aug 15, 2017
1.Identification
1.1 GHS Product identifier
| Product name | 1-(3-methoxyphenyl)-N-methylpropane-2-amine |
|---|
1.2 Other means of identification
| Product number | – |
|---|---|
| Other names | [2-(3-Methoxy-phenyl)-1-methyl-ethyl]-methyl-amine |
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). |
More Details:93675-25-3 SDS
93675-25-3Upstream product
93675-25-3Downstream Products
93675-25-3Relevant academic research and scientific papers
Controlling stereoselectivity by enzymatic and chemical means to access enantiomerically pure (1S,3R)-1-benzyl-2,3-dimethyl-1,2,3,4- tetrahydroisoquinoline derivatives
Orden, Alejandro A.,Schrittwieser, Joerg H.,Resch, Verena,Mutti, Francesco G.,Kroutil, Wolfgang
, p. 744 – 749 (2013/07/25)
A chemoenzymatic strategy for the synthesis of enantiomerically pure novel alkaloids (1S,3R)-1-benzyl-2,3-dimethyl-1,2,3,4-tetrahydroisoquinolines is presented. The key steps are the biocatalytic stereoselective reductive amination of substituted 1-phenyl
See also
- Substituted methoxyphenethylamine
- para-Methoxyamphetamine
- Fenfluramine
- 2-Methoxymethamphetamine
- 3-Chloromethamphetamine
- 3-Methoxy-4-methylamphetamine
- 4-Fluoromethamphetamine
- 4-Methylmethamphetamine
References
- Dal Cason TA (June 2001). “A re-examination of the mono-methoxy positional ring isomers of amphetamine, methamphetamine and phenyl-2-propanone”. Forensic Science International. 119 (2): 168–194. doi:10.1016/S0379-0738(00)00425-4. PMID11376983.
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