Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H5ClO2 |
| Molecular Weight | 120.534 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC(=O)OCC=C
InChI
InChIKey=CAEWJEXPFKNBQL-UHFFFAOYSA-N
InChI=1S/C4H5ClO2/c1-2-3-7-4(5)6/h2H,1,3H2
| Molecular Formula | C4H5ClO2 |
| Molecular Weight | 120.534 |
| 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 |
|---|---|---|
| Regio- and stereoselective anomeric esterification of glucopyranose 1,2-diols and a facile preparation of 2-O-acetylated glucopyranosyl trichloroacetimidates from the corresponding 1,2-diols. | 2007 May 7 |
|
| Synthetic studies on formamidopyrimidines related to clofarabine. | 2008 Aug |
|
| Allyl 4-hydroxy-phenyl carbonate. | 2009 Jun 17 |
|
| Diallyl 5-[(4-hexyl-oxyphen-yl)imino-meth-yl]-m-phenyl-ene dicarbonate. | 2009 Oct 23 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:55:15 GMT 2023
by
admin
on
Sat Dec 16 08:55:15 GMT 2023
|
| Record UNII |
7672CAR559
|
| Record Status |
Validated (UNII)
|
| Record Version |
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DTXSID2051972
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7672CAR559
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2937-50-0
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