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Details

Stereochemistry ACHIRAL
Molecular Formula C2H2Cl2O
Molecular Weight 112.943
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DICHLOROACETALDEHYDE

SMILES

ClC(Cl)C=O

InChI

InChIKey=NWQWQKUXRJYXFH-UHFFFAOYSA-N
InChI=1S/C2H2Cl2O/c3-2(4)1-5/h1-2H

HIDE SMILES / InChI

Molecular Formula C2H2Cl2O
Molecular Weight 112.943
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Chloramphenicol biosynthesis: the structure of CmlS, a flavin-dependent halogenase showing a covalent flavin-aspartate bond.
2010-03-19
Xenobiotic exposure and autoimmune hepatitis.
2010
A structurally diverse series of aluminum chloride alkoxides [Cl(x)Al(mu-OR)(y)](n) (R = (n)Bu, (c)Hex, Ph, 2,4-(t)Bu2C6H3).
2009-09-07
Disinfection byproduct formation and fractionation behavior of natural organic matter surrogates.
2009-08-01
A structural study of the interaction between the Dr haemagglutinin DraE and derivatives of chloramphenicol.
2009-06
Occurrence of a new generation of disinfection byproducts.
2006-12-01
Halogenated acetaldehydes: analysis, stability and fate in drinking water.
2006-07
Pulmonary bronchiolar cytotoxicity and formation of dichloroacetyl lysine protein adducts in mice treated with trichloroethylene.
2006-02
Bioactivation of 1,1-dichloroethylene to its epoxide by CYP2E1 and CYP2F enzymes.
2004-09
Biosynthesis of the dichloroacetyl component of chloramphenicol in Streptomyces venezuelae ISP5230: genes required for halogenation.
2004-01
Evidence for trichloroethylene bioactivation and adduct formation in the rat epididymis and efferent ducts.
2003-09
Analysis of 6-(2,2-Dichloroacetamido)chrysene interaction with the hypoxanthine phosphoribosyltransferase from Trypanosoma cruzi.
2003-06-05
Reaction of trichloroethylene and trichloroethylene oxide with cytochrome P450 enzymes: inactivation and sites of modification.
2001-04
Mechanisms of 1,1-dichloroethylene-induced cytotoxicity in lung and liver.
2001-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:52:27 GMT 2025
Edited
by admin
on Mon Mar 31 18:52:27 GMT 2025
Record UNII
9GT3DHH725
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-5207
Preferred Name English
DICHLOROACETALDEHYDE
HSDB  
Systematic Name English
DICHLOROACETALDEHYDE, 2,2-
Systematic Name English
DICHLOROACETALDEHYDE [HSDB]
Common Name English
Code System Code Type Description
PUBCHEM
6576
Created by admin on Mon Mar 31 18:52:27 GMT 2025 , Edited by admin on Mon Mar 31 18:52:27 GMT 2025
PRIMARY
NSC
5207
Created by admin on Mon Mar 31 18:52:27 GMT 2025 , Edited by admin on Mon Mar 31 18:52:27 GMT 2025
PRIMARY
CAS
79-02-7
Created by admin on Mon Mar 31 18:52:27 GMT 2025 , Edited by admin on Mon Mar 31 18:52:27 GMT 2025
PRIMARY
HSDB
5226
Created by admin on Mon Mar 31 18:52:27 GMT 2025 , Edited by admin on Mon Mar 31 18:52:27 GMT 2025
PRIMARY
EPA CompTox
DTXSID3021560
Created by admin on Mon Mar 31 18:52:27 GMT 2025 , Edited by admin on Mon Mar 31 18:52:27 GMT 2025
PRIMARY
FDA UNII
9GT3DHH725
Created by admin on Mon Mar 31 18:52:27 GMT 2025 , Edited by admin on Mon Mar 31 18:52:27 GMT 2025
PRIMARY
MESH
C015798
Created by admin on Mon Mar 31 18:52:27 GMT 2025 , Edited by admin on Mon Mar 31 18:52:27 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-169-5
Created by admin on Mon Mar 31 18:52:27 GMT 2025 , Edited by admin on Mon Mar 31 18:52:27 GMT 2025
PRIMARY