Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H12ClNO2 |
| Molecular Weight | 213.661 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=O)OC1=C(Cl)C=C(C)C(C)=C1
InChI
InChIKey=QRTXZGIQTYDABO-UHFFFAOYSA-N
InChI=1S/C10H12ClNO2/c1-6-4-8(11)9(5-7(6)2)14-10(13)12-3/h4-5H,1-3H3,(H,12,13)
| Molecular Formula | C10H12ClNO2 |
| Molecular Weight | 213.661 |
| 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 |
|---|---|---|
| Optically active (aR)- and (aS)-linear and vaulted biaryl ligands: deracemization versus oxidative dimerization. | 2009-10-14 |
|
| An efficient synthesis of (-)-chloramphenicol via asymmetric catalytic aziridination: a comparison of catalysts prepared from triphenylborate and various linear and vaulted biaryls. | 2001-11-15 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:31:15 GMT 2025
by
admin
on
Mon Mar 31 19:31:15 GMT 2025
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| Record UNII |
M05Z0Q9XTF
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| Record Status |
Validated (UNII)
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EPA PESTICIDE CODE |
219100
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