Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C20H17ClO3 |
| Molecular Weight | 340.8 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC3(CC1(CO1)C2=CC=CC(Cl)=C2)C(=O)C4=CC=CC=C4C3=O
InChI
InChIKey=PMAAYIYCDXGUAP-UHFFFAOYSA-N
InChI=1S/C20H17ClO3/c1-2-19(17(22)15-8-3-4-9-16(15)18(19)23)11-20(12-24-20)13-6-5-7-14(21)10-13/h3-10H,2,11-12H2,1H3
| Molecular Formula | C20H17ClO3 |
| Molecular Weight | 340.8 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Comparative study of human and mouse pregnane X receptor agonistic activity in 200 pesticides using in vitro reporter gene assays. | 2011-02-27 |
|
| Practical asymmetric synthesis of the herbicide (S)-indanofan via lipase-catalyzed kinetic resolution of a diol and stereoselective acid-catalyzed hydrolysis of a chiral epoxide. | 2002-05-03 |
|
| Inhibition of very-long-chain fatty acid formation by indanofan, 2-[2-(3-chlorophenyl)oxiran-2-ylmethyl]-2-ethylindan-1,3-dione, and its relatives. | 2002-04-03 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:18:49 GMT 2025
by
admin
on
Mon Mar 31 22:18:49 GMT 2025
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| Record UNII |
Z5WQ384U76
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| Record Status |
Validated (UNII)
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| Record Version |
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Z5WQ384U76
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11046097
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indanofan
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m6243
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133220-30-1
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