Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H5ClO2 |
| Molecular Weight | 108.524 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCC(=O)CCl
InChI
InChIKey=JWZYQAITGQPZNM-UHFFFAOYSA-N
InChI=1S/C3H5ClO2/c4-1-3(6)2-5/h5H,1-2H2
| Molecular Formula | C3H5ClO2 |
| Molecular Weight | 108.524 |
| 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 |
|---|---|---|
| Genome-wide profiling of gene expression in the epididymis of alpha-chlorohydrin-induced infertile rats using an oligonucleotide microarray. | 2010-04-22 |
|
| Structure of insoluble rat sperm glyceraldehyde-3-phosphate dehydrogenase (GAPDH) via heterotetramer formation with Escherichia coli GAPDH reveals target for contraceptive design. | 2009-08-21 |
|
| Lack of antifertility properties of novel halogenated glycolytic inhibitors and the urinary excretion and metabolism of 1,6-dichloro-1,6-dideoxy-D-fructofuranose in the male rat. | 2002-06 |
|
| The effect of (R,S)-ornidazole on the fertility of male mice and the excretion and metabolism of 36Cl-(R,S)-ornidazole and 36Cl-(R,S)-alpha-chlorohydrin in male mice and rats. | 2002-04 |
|
| Susceptibility of glycolytic enzyme activity and motility of spermatozoa from rat, mouse, and human to inhibition by proven and putative chlorinated antifertility compounds in vitro. | 2001-05-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:54:27 GMT 2025
by
admin
on
Mon Mar 31 18:54:27 GMT 2025
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| Record UNII |
QU742J268W
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| Record Status |
Validated (UNII)
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| Record Version |
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246-239-6
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90494
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QU742J268W
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C027160
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DTXSID90179178
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24423-98-1
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