42932-20-7

Basic information

• Product Name: N-formylmethamphetamine
• Synonyms: N-formylmethamphetamine;rac N-ForMyl MethaMphetaMine;N-Formyl-methylamphetamine;1-Phenyl-2-(N-Methyl-N- forMylaMino)propane;N-Methyl-N-(1-Methyl-2-phenylethyl)forMaMide;N-methyl-N-(1-phenylpropan-2-yl)formamide
• CAS NO: 42932-20-7
• Molecular Formula: C₁₁H₁₅NO
• Molecular Weight: 177.24
• Product Categories: Aromatics;Impurities;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 42932-20-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 325.4°Cat760mmHg
• Flash Point: 121.7°C
• Appearance: /
• Density: 1.002g/cm³
• Vapor Pressure: 0.000231mmHg at 25°C
• Refractive Index: 1.518
• CAS DataBase Reference: N-formylmethamphetamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-formylmethamphetamine(42932-20-7)
• EPA Substance Registry System: N-formylmethamphetamine(42932-20-7)

Safety Data

• RIDADR: 2810
• HazardClass: 6.1(b)
• PackingGroup: III
• Hazardous Substances Data: 42932-20-7(Hazardous Substances Data)

Usage

Uses

An impurity of Methamphetamine (M258795). Controlled substance.

InChI:InChI=1/C11H15NO/c1-10(12(2)9-13)8-11-6-4-3-5-7-11/h3-7,9-10H,8H2,1-2H3

Upstream product

• 7632-10-2 methamphetamin 
• 64-18-6 formic acid 
• 593-51-1 methylamine hydrochloride 
• 103-79-7 1-phenyl-acetone 
• 103-82-2 phenylacetic acid 
• 123-39-7 N-Methylformamide 
• 1668-82-2 (2S,4S)-3,4-dimethyl-5-phenyl-1,3-oxazolidine 
• 102732-70-7 <5-(4-Chlorphenyl)-2-furylmethyl>-methyl-(1-methyl-2-phenyl-ethyl)-amin 
• 102732-71-8 -(5-phenyl-2-furylmethyl)-amin 
• 67-56-1 methanol 
• 102732-72-9 <5-(4-Methoxyphenyl)-2-furylmethyl>-methyl-(1-methyl-2-phenyl-ethyl)-amin 

Downstream Products

• 7632-10-2 methamphetamin 

Relevant articles and documents

Compositions and Methods for Treating Cocaine, Nicotine, and Methamphetamine Dependence

This invention provides a composition of matter comprising a plurality of cocaine-succinyl-BSA, wherein the average ratio of cocaine-succinyl moieties to BSA is at least 7.0. This invention also provides a composition of matter comprising a plurality of nicotine-5-succinyl-BSA, wherein the average ratio of nicotine-5-succinyl moieties to BSA is at least 7.0. This invention further provides a composition of matter comprising a plurality of methamphetamine-5-succinyl-BSA, wherein the average ratio of methamphetamine-5-succinyl moieties to BSA is at least 7.0. This invention still further provides related pharmaceutical compositions, therapeutic methods, prophylactic methods, synthetic methods, and articles of manufacture.

Determination of the synthetic origin of methamphetamine samples by 2H NMR spectroscopy

Samples of methamphetamine, prepared according to the most common synthetic pathways, were submitted to natural-abundance 2H NMR spectroscopy. The deuterium content at the various sites of the molecule was found to depend on its synthetic history. The technique provides a chemical fingerprint of methamphetamine samples and can give hints to trace back the starting materials and the synthetic procedures.

Cleavage reactions of the anorectic drug furfenorex

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