93138-61-5

Basic information

• Product Name: C-(1-BENZYL-PYRROLIDIN-3-YL)-METHYLAMINE
• Synonyms: 1-BENZYL-3-AMINOMETHYLPYRROLIDINE;3-AMINOMETHYL-1-BENZYL-PYRROLIDINE;AKOS BB-9094;CHEMBRDG-BB 4003808;C-(1-BENZYL-PYRROLIDIN-3-YL)-METHYLAMINE;TIMTEC-BB SBB010842;(1-Benzylpyrrolidin-3-yl)methylamine;1-(1-benzylpyrrolidin-3-yl)methanamine
• CAS NO: 93138-61-5
• Molecular Formula: C₁₂H₁₈N₂
• Molecular Weight: 190.28
• Product Categories: pharmacetical;Aminomethyl's;Pyrrolidines
• Mol File: 93138-61-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 284.3 °C at 760 mmHg
• Flash Point: 115.3 °C
• Appearance: /
• Density: 1.04 g/cm³
• Vapor Pressure: 0.003mmHg at 25°C
• PKA: 10.12±0.29(Predicted)
• CAS DataBase Reference: C-(1-BENZYL-PYRROLIDIN-3-YL)-METHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: C-(1-BENZYL-PYRROLIDIN-3-YL)-METHYLAMINE(93138-61-5)
• EPA Substance Registry System: C-(1-BENZYL-PYRROLIDIN-3-YL)-METHYLAMINE(93138-61-5)

Safety Data

• Hazard Codes: Xi,T
• Statements: 25
• Safety Statements: 45
• HazardClass: IRRITANT
• Hazardous Substances Data: 93138-61-5(Hazardous Substances Data)

Usage

General Description

C-(1-benzyl-pyrrolidin-3-yl)-methylamine is a chemical compound with the molecular formula C14H20N2. It is a derivative of pyrrolidine and contains a benzyl group and a methylamine group. C-(1-BENZYL-PYRROLIDIN-3-YL)-METHYLAMINE is commonly used in pharmaceutical research and drug development due to its potential therapeutic properties. It may act as a central nervous system stimulant and have applications in the treatment of various neurological and psychiatric disorders. Additionally, it could also have potential use in the synthesis of other organic compounds. However, as with any chemical compound, it is important to handle C-(1-benzyl-pyrrolidin-3-yl)-methylamine with care and follow proper safety protocols when working with it in a laboratory setting.

InChI:InChI=1/C12H18N2/c13-8-12-6-7-14(10-12)9-11-4-2-1-3-5-11/h1-5,12H,6-10,13H2/p+2/t12-/m1/s1

Upstream product

• 5731-17-9 1-(Phenylmethyl)-3-pyrrolidinemethanol 
• 10603-52-8 1-benzyl-pyrrolidine-3-carbonitrile 
• 116041-19-1 1-benzyl 5-oxo-pyrrolidine-3-carboxamide 
• 7757-82-6 sodium sulfate 

Downstream Products

• 155497-10-2 (1-benzyl-pyrrolidin-3-ylmethyl)-carbamic acid tert-butyl ester 
• 849632-74-2 2,2,2-trifluoro-N-{[(3RS)-1-(phenylmethyl)-3-pyrrolidinyl]methyl}acetamide 
• 270912-72-6 tert-butyl 3-(aminomethyl)pyrrolidine-1-carboxylate 
• 1301189-87-6 3-{[((3RS)-1-{[(1,1-dimethylethyl)oxy]carbonyl}-3-pyrrolidinyl)methyl]amino}-4-nitrobenzoic acid 
• 1301189-89-8 2-(4-biphenylyl)-1-[((3R₅)-1-{[(1,1-dimethylethyl)oxy]carbonyl}-3-pyrrolidinyl)methyl]-1H-benzimidazole-6-carboxylic acid 
• 1301189-91-2 1,1-dimethylethyl (3RS)-3-({2-(4-biphenylyl)-6-[(methylamino)carbonyl]-1H-benzimidazol-1-yl}methyl)-1-pyrrolidinecarboxylate 
• 1301189-92-3 2-(4-biphenylyl)-N-methyl-1-[(3RS)-3-pyrrolidinylmethyl]-1H-benzimidazole-6-carboxamide 
• 1301188-36-2 2-(4-biphenylyl)-1-({(3RS)-1-[(dimethylamino)carbonyl]-3-pyrrolidinyl}methyl)-N-methyl-1H-benzimidazole-6-carboxamide 
• 1301188-37-3 2-(4-biphenylyl)-N-methyl-1-({(3RS)-1-[(3-methyl-5-isoxazolyl)carbonyl]-3-pyrrolidinyl}methyl)-1H-benzimidazole-6-carboxamide 
• 1426095-67-1 N-methyl-N-(3(RS)-pyrrolidinylmethyl)-4-biphenylcarboxamide 
• 1303967-33-0 1-dimethylethyl 3(RS)-{[(1-methylethyl)amino]methyl}-1-pyrrolidinecarboxylate 
• 1426095-68-2 1,1-dimethylethyl (3RS)-[({[3-(methyloxy)-4-biphenylyl]carbonyl}amino)methyl]-1-pyrrolidinecarboxylate 
• 1426095-69-3 N-methyl-3-(methyloxy)-N-(3(RS)-pyrrolidinylmethyl)-4-biphenylcarboxamide 
• 1426094-94-1 N-{[(3RS)-1-cyclopropylcarbonyl-3-pyrrolidinyl]methyl}-N-methyl-4-biphenylcarboxamide 

Relevant articles and documents

Indole, azaindole and related heterocyclic pyrrolidine derivatives

This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with amido piperazine derivatives. These compounds possess unique antiviral activity

Synthesis and pharmacological evaluation of carboxamide derivatives as selective serotoninergic 5-HT4 receptor agonists (European Journal of Medicinal Chemistry (1999) 34 (329-987))

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