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Details

Stereochemistry ACHIRAL
Molecular Formula C4H7ClO2
Molecular Weight 122.55
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Ethyl chloroacetate

SMILES

CCOC(=O)CCl

InChI

InChIKey=VEUUMBGHMNQHGO-UHFFFAOYSA-N
InChI=1S/C4H7ClO2/c1-2-7-4(6)3-5/h2-3H2,1H3

HIDE SMILES / InChI
Molecular Formula C4H7ClO2
Molecular Weight 122.55
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Bis(2-{2-[2-(benzyl-carbamo-yl)phen-oxy]acetamido}-eth-yl)ammonium nitrate ethanol disolvate.
2010-12-24
Ethyl 2-(1H-1,2,3-benzotriazol-1-yl)acetate.
2010-12-15
N-(3-Octyl-4-oxo-1,3-thia-zolidin-2-yl-idene)benzamide.
2010-11-24
Ethyl 2-(2-methyl-4-nitro-1H-imidazol-1-yl)acetate.
2010-09-25
Ethyl 2-(2-oxo-4-phenyl-2,3-dihydro-1H-1,5-benzodiazepin-1-yl)acetate.
2010-07-21
Infrared spectroscopic studies of the conformation in ethyl alpha-haloacetates in the vapor, liquid and solid phases.
2010-07
N-(3-Butyl-4-oxo-1,3-thia-zolidin-2-yl-idene)benzamide.
2010-06-26
1-(4-Methoxy-phen-yl)imidazolidine-2,4-dione.
2010-05-12
Synthesis and biological activities of some novel triazoloquinazolines and triazinoquinazolines containing benzenesulfonamide moieties.
2010
2-Phenoxy-acetohydrazide.
2009-12-04
2-(2-Chloro-phen-oxy)acetohydrazide.
2009-12-04
New insights into the design of inhibitors of human S-adenosylmethionine decarboxylase: studies of adenine C8 substitution in structural analogues of S-adenosylmethionine.
2009-03-12
Ethyl 2-(4-chloro-2-oxo-2,3-dihydro-1,3-benzothia-zol-3-yl)acetate.
2009-03-06
Ethoxy-carbonyl-methyl ursolate.
2008-11-29
Synthesis and Activity Evaluation of 2-(1-naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles.
2008-11
Synthesis and Biological Screening of 5-{[(4,6-Disubstituted pyrimidine-2-yl)thio]methyl}-N-phenyl-1,3,4-thiadiazol-2-amines.
2008-09
Ethyl 2-[(Z)-2-cyano-imino-1,3-thiazolidin-3-yl]acetate.
2008-06-07
Synthesis, molecular structure and spectral properties of quaternary ammonium derivatives of 1,1-dimethyl-1,3-propylenediamine.
2008-02-15
Ethyl 5-(ethoxy-carbon-yl)-3-(4-methoxy-phen-yl)-1H-pyrazole-1-acetate.
2007-12-06
An easy synthesis of 5-functionally substituted ethyl 4-amino-1-aryl- pyrazolo-3-carboxylates: interesting precursors to sildenafil analogues.
2007-05-01
Synthesis and antimicrobial activities of some novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines carrying thioalkyl and sulphonyl phenoxy moieties.
2007-04
Microwave-assisted organic synthesis of 3-(D-Gluco-pentitol-1-yl)-1H-1,2,4-triazole.
2006-03
Anti-tumor and proapoptotic effect of novel synthetic benzophenone analogues in Ehrlich ascites tumor cells.
2006-01-15
Synthesis and antimicrobial study of novel heterocyclic compounds from hydroxybenzophenones.
2005-11
Synthesis of 2-(aminocarbonylmethylthio)-1H-imidazoles as novel Capravirine analogues.
2005-07-01
Syntheses and evaluation of antioxidant activity of sydnonyl substituted thiazolidinone and thiazoline derivatives.
2004-09-01
Nitrosation of glycine ethyl ester and ethyl diazoacetate to give the alkylating agent and mutagen ethyl chloro(hydroximino)acetate.
2004-03
Synthesis of hapten and conjugates of coumestrol and development of immunoassay.
2003-12
Pharmaco-economical analysis of the treatment with antibiotics in a surgery department.
2003-05
Synthesis of some new pyrimidine and fused pyrimidine derivatives (Part 2).
2003-04
Patents

Patents

04022908
3
04045469
2
04103085
2
04241097
1
04259214
1
04399300
4
04443624
4
04481268
1
04672066
1
04898862
1
04914093
1
05192357
1
05380721
4
05422360
1
05457205
1
05478827
1
05559158
3
05583232
3
05624931
1
05883262
1
06150530
3
06221335
1
06313296
2
06362182
3
06528653
1
06667404
3
06723722
2
07227020
1
07241893
2
07371773
1
07612114
20
07829568
1
07846923
1
08383630
1
08394799
36
08785456
2
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:58:13 GMT 2025
Edited
by admin
on Mon Mar 31 19:58:13 GMT 2025
Record UNII
6H07TEH4TF
Record Status Validated (UNII)
Record Version
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Name Type Language
Ethyl chloroacetate
HSDB   MI  
Systematic Name English
NSC-8833
Preferred Name English
2-CHLOROACETIC ACID ETHYL ESTER
Systematic Name English
ETHYL CHLOROACETATE [MI]
Common Name English
ETHYL CHLOROACETATE [HSDB]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID4026715
Created by admin on Mon Mar 31 19:58:13 GMT 2025 , Edited by admin on Mon Mar 31 19:58:13 GMT 2025
PRIMARY
FDA UNII
6H07TEH4TF
Created by admin on Mon Mar 31 19:58:13 GMT 2025 , Edited by admin on Mon Mar 31 19:58:13 GMT 2025
PRIMARY
HSDB
408
Created by admin on Mon Mar 31 19:58:13 GMT 2025 , Edited by admin on Mon Mar 31 19:58:13 GMT 2025
PRIMARY
CAS
105-39-5
Created by admin on Mon Mar 31 19:58:13 GMT 2025 , Edited by admin on Mon Mar 31 19:58:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-294-0
Created by admin on Mon Mar 31 19:58:13 GMT 2025 , Edited by admin on Mon Mar 31 19:58:13 GMT 2025
PRIMARY
PUBCHEM
7751
Created by admin on Mon Mar 31 19:58:13 GMT 2025 , Edited by admin on Mon Mar 31 19:58:13 GMT 2025
PRIMARY
MERCK INDEX
m5108
Created by admin on Mon Mar 31 19:58:13 GMT 2025 , Edited by admin on Mon Mar 31 19:58:13 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
ETHYL CHLOROACETATE
Created by admin on Mon Mar 31 19:58:13 GMT 2025 , Edited by admin on Mon Mar 31 19:58:13 GMT 2025
PRIMARY
NSC
8833
Created by admin on Mon Mar 31 19:58:13 GMT 2025 , Edited by admin on Mon Mar 31 19:58:13 GMT 2025
PRIMARY
NIH
NCATS
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