Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H10ClO3P |
| Molecular Weight | 268.633 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClP(=O)(OC1=CC=CC=C1)OC2=CC=CC=C2
InChI
InChIKey=BHIIGRBMZRSDRI-UHFFFAOYSA-N
InChI=1S/C12H10ClO3P/c13-17(14,15-11-7-3-1-4-8-11)16-12-9-5-2-6-10-12/h1-10H
| Molecular Formula | C12H10ClO3P |
| Molecular Weight | 268.633 |
| 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 |
|---|---|---|
| Carbon dioxide as a carbonylating agent in the synthesis of 2-oxazolidinones, 2-oxazinones, and cyclic ureas: scope and limitations. | 2010-05-07 |
|
| Diphenyl (benzyl-amido)phosphate. | 2009-12-19 |
|
| Efficient chemical synthesis of both anomers of ADP L-glycero- and D-glycero-D-manno-heptopyranose. | 2003-11-14 |
|
| Synthesis of P(1)-Citronellyl-P(2)-alpha-D-pyranosyl pyrophosphates as potential substrates for the E. coli undecaprenyl-pyrophosphoryl-N-acetylglucoseaminyl transferase MurG. | 2001-12-17 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:10:34 GMT 2025
by
admin
on
Mon Mar 31 21:10:34 GMT 2025
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| Record UNII |
1KEE9757OT
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| Record Status |
Validated (UNII)
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