PROPYL CHLORIDE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C3H7Cl
Molecular Weight	78.541
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CCCCl

InChI

InChIKey=SNMVRZFUUCLYTO-UHFFFAOYSA-N

InChI=1S/C3H7Cl/c1-2-3-4/h2-3H2,1H3

HIDE SMILES / InChI

Molecular Formula	C3H7Cl
Molecular Weight	78.541
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Synthesis and identification of products derived from the metabolism of the carcinostatic 1-(2-chloroethyl)-3-(trans-4-methylcyclohexyl)-1-nitrosourea by rat liver microsomes.	1979 Mar	427763
[Anti-corrosive effect of pesticides in soil corrosion conditions].	2001 Jul-Aug	11692682
Adsorption of chloroacetanilide herbicides on soil and its components. III. Influence of clay acidity, humic acid coating and herbicide structure on acetanilide herbicide adsorption on homoionic clays.	2002 Apr	12046284
4-Hydroxybenzoate uptake in Klebsiella planticola strain DSZ1 is driven by DeltapH.	2002 Jan	11727038
Influence of herbicide structure, clay acidity, and humic acid coating on acetanilide herbicide adsorption on homoionic clays.	2002 Jul 3	12083874
Nucleophilic aliphatic substitution reactions of propachlor, alachlor, and metolachlor with bisulfide (HS-) and polysulfides (Sn2-).	2002 Oct 1	12380076
Mutagenicity and cross-linking activity of chloroalkylnitrosamines, possible new antitumor lead compounds.	2003 Jul	12840106
Studies on quinazolines. 11. Intramolecular imidate-amide rearrangement of 2-substituted 4-(omega-chloroalkoxy)quinazoline derivatives. 1,3 -O --> N shift of chloroalkyl groups via cyclic 1,3-azaoxonium intermediates.	2003 Mar 21	12636427
Transformation of herbicide propachlor by an agrochemical thiourea.	2004 Dec 15	15669349
Voltammetric sensor for general purpose organohalide detection at picogram per liter concentrations based on a simple collector-generator method.	2004 Feb 1	14750886
Kinetics and mechanism of the nucleophilic displacement reactions of chloroacetanilide herbicides: investigation of alpha-substituent effects.	2004 May 19	15137847
Correlation analyses for bimolecular nucleophilic substitution reactions of chloroacetanilide herbicides and their structural analogs with environmentally relevant nucleophiles.	2005 Oct	16268142
Degradation of chloroacetanilide herbicides by anodic fenton treatment.	2006 Apr 5	16569056
Preparation, structure and thermal stability of onium- and amino-functionalized silicas for the use as catalysts supports.	2006 Oct 1	16857208
Characterization of glutathione conjugates of chloroacetanilide pesticides using ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry and liquid chromatography/ion trap mass spectrometry.	2007	18004742
Effects of relative humidity on chloroacetanilide and dinitroaniline herbicide desorption from agricultural PM2.5 on quartz fiber filters.	2007 Jun 1	17612158
Characterization of acetanilide herbicides degrading bacteria isolated from tea garden soil.	2008 Apr	17661128
1-Methyl-1-propyl-pyrrolidinium chloride.	2008 Feb 29	21201968
Specific interactions of chloroacetanilide herbicides with human ABC transporter proteins.	2008 Jun 3	18433974
Degradation of acetochlor by four microbial communities.	2008 Nov	18331792
The watershed as a conceptual framework for the study of environmental and human health.	2009 Feb 18	20508751
2-Chloro-N-isopropyl-N-phenyl-acetamide.	2010 Jul 14	21588328

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:39:28 GMT 2023` Edited by `admin` on `Fri Dec 15 18:39:28 GMT 2023`
Record UNII	TUV7462NWK
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

PROPYL CHLORIDE

Systematic Name

English

1-CHLOROPROPANE [HSDB]

Common Name

English

1-CHLOROPROPANE

Systematic Name

English

PROPYL CHLORIDE [MI]

Common Name

English

PROPANE, 1-CHLORO-

Systematic Name

English

CHLOROPROPANE

Systematic Name

English

N-PROPYL CHLORIDE

Common Name

English

Code System Code Type Description

ECHA (EC/EINECS)

208-749-7