Cyclopropylamine

Details

Stereochemistry	ACHIRAL
Molecular Formula	C3H7N
Molecular Weight	57.0944
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

NC1CC1

InChI

InChIKey=HTJDQJBWANPRPF-UHFFFAOYSA-N

InChI=1S/C3H7N/c4-3-1-2-3/h3H,1-2,4H2

HIDE SMILES / InChI

Approval Year

PubMed

Show entries

Title	Date	PubMed
Bacterial degradation of N-cyclopropylmelamine. The steps to ring cleavage.	1984 Sep 1	6477516
Effect of mobile phase amine additives on enantioselectivity for phenylalanine analogs.	2001 Aug 24	11572398
Enzymatic N-dealkylation of an N-cyclopropylamine: an unusual fate for the cyclopropyl group.	2001 Jan 17	11456529
Three-component aldimine addition--cyclopropanation. an efficient new methodology for amino cyclopropane synthesis.	2001 May 30	11457353
Radical cation-mediated annulation. Stereoselective construction of bicyclo[5.3.0]decan-3-ones by aerobic oxidation of cyclopropylamines.	2001 Nov 14	11697988

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Name

Type

Language

NSC-56127

Preferred Name

English

Cyclopropylamine

Systematic Name

English

CYCLOPROPANAMINE

Systematic Name

English

AMINOCYCLOPROPANE

Systematic Name

English

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Code System

Code

Type

Description

FDA UNII

8PR8XTH1X1

PRIMARY

MESH

C067351

PRIMARY

ECHA (EC/EINECS)

212-142-2

PRIMARY

CAS

765-30-0

PRIMARY

PUBCHEM

69828

PRIMARY

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SUBSTANCE RECORD


					8PR8XTH1X1

Cyclopropylamine

SMILES

InChI

Approval Year

PubMed

Patents