U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C2H6ClN
Molecular Weight 79.529
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-CHLOROETHYLAMINE

SMILES

NCCCl

InChI

InChIKey=VKPPFDPXZWFDFA-UHFFFAOYSA-N
InChI=1S/C2H6ClN/c3-1-2-4/h1-2,4H2

HIDE SMILES / InChI

Molecular Formula C2H6ClN
Molecular Weight 79.529
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A new inhibitor design strategy for carboxypeptidase A as exemplified by N-(2-chloroethyl)-N-methylphenylalanine.
2001 Feb
Identification of new aqueous chemical degradation products of isophosphoramide mustard.
2001 Jun
Structure--activity relationships among novel phenoxybenzamine-related beta-chloroethylamines.
2002 May
Thiosugar nucleosides. Synthesis and biological activity of 1,3,4-thiadiazole, thiazoline and thiourea derivatives of 5-thio-D-glucose.
2004
Conjugates of phthalocyanines with oligonucleotides as reagents for sensitized or catalytic DNA modification.
2006
Kinetic study of DNA modification by phthalocyanine derivative of the oligonucleotide.
2006
Genotoxicants target distinct molecular networks in neonatal neurons.
2006 Nov
Synthesis of DNA-directed pyrrolidinyl and piperidinyl confined alkylating chloroalkylaminoanthraquinones: potential for development of tumor-selective N-oxides.
2006 Nov 30
Antihypertensive activity of chitin derivatives.
2006 Oct 15
Alkylation potency and protein specificity of aromatic urea derivatives and bioisosteres as potential irreversible antagonists of the colchicine-binding site.
2007 Jul 1
Synthesis and in vitro antiproliferative activity of new 1,3-(oxytetraethylenoxy)-cyclotriphosphazene derivatives.
2007 May-Jun
The new analogues of nitrogen mustard with one, two or three 2-chloroethylamino fragments. Reactions with nucleophiles.
2008 Nov-Dec
DNA repair modulates the vulnerability of the developing brain to alkylating agents.
2009 Mar 1
Determination of silver(I) by differential pulse voltammetry using a glassy carbon electrode modified with synthesized N-(2-aminoethyl)-4,4'-bipyridine.
2010
1-Methyl-4H-3,1-benzoxazine-2,4(1H)dione.
2010 Feb 20
Angiotensin-I-converting enzyme (ACE) inhibitors from marine resources: prospects in the pharmaceutical industry.
2010 Mar 31
(E)-2,4-Dichloro-6-{1-[(2-chloro-eth-yl)imino]-eth-yl}phenol.
2010 Nov 10
Complexation properties and synthesis of a novel Schiff base with triphenylene nucleus.
2010 Nov 15
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:06:05 GMT 2023
Edited
by admin
on Sat Dec 16 01:06:05 GMT 2023
Record UNII
P7YLY3O329
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-CHLOROETHYLAMINE
Systematic Name English
CHLOROETHYLAMINE
Systematic Name English
1-CHLORO-2-AMINOETHANE
Systematic Name English
ETHANAMINE, 2-CHLORO-
Systematic Name English
NSC-10871
Code English
.BETA.-CHLOROETHYLAMINE
Systematic Name English
CARMUSTINE RELATED COMPOUND, 2-CHLOROETHYLAMINE-
Common Name English
2-AMINOETHYL CHLORIDE
Systematic Name English
2-CHLOROETHANAMINE
Systematic Name English
IFOSFAMIDE IMPURITY C [EP IMPURITY]
Common Name English
1-AMINO-2-CHLOROETHANE
Systematic Name English
Code System Code Type Description
CAS
689-98-5
Created by admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
PRIMARY
NSC
10871
Created by admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
PRIMARY
PUBCHEM
13369
Created by admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
PRIMARY
EPA CompTox
DTXSID10218977
Created by admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
PRIMARY
FDA UNII
P7YLY3O329
Created by admin on Sat Dec 16 01:06:06 GMT 2023 , Edited by admin on Sat Dec 16 01:06:06 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE
Related Record Type Details
PARENT -> IMPURITY
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP