Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H12O |
Molecular Weight | 136.191 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=CC(O)=CC=C1
InChI
InChIKey=VLJSLTNSFSOYQR-UHFFFAOYSA-N
InChI=1S/C9H12O/c1-7(2)8-4-3-5-9(10)6-8/h3-7,10H,1-2H3
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Testing electrostatic complementarity in enzyme catalysis: hydrogen bonding in the ketosteroid isomerase oxyanion hole. | 2006 Apr |
|
Responses of Tabanidae (Diptera) to canopy traps baited with 4-methylphenol, 3-isopropylphenol, and naphthalene. | 2007 Dec |
|
Isolation and characterization of a novel 2-sec-butylphenol-degrading bacterium Pseudomonas sp. strain MS-1. | 2010 Apr |
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Code System | Code | Type | Description | ||
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C028686
Created by
admin on Sat Dec 16 06:35:04 GMT 2023 , Edited by admin on Sat Dec 16 06:35:04 GMT 2023
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12059
Created by
admin on Sat Dec 16 06:35:04 GMT 2023 , Edited by admin on Sat Dec 16 06:35:04 GMT 2023
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618-45-1
Created by
admin on Sat Dec 16 06:35:04 GMT 2023 , Edited by admin on Sat Dec 16 06:35:04 GMT 2023
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2209
Created by
admin on Sat Dec 16 06:35:04 GMT 2023 , Edited by admin on Sat Dec 16 06:35:04 GMT 2023
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ERD00478GH
Created by
admin on Sat Dec 16 06:35:04 GMT 2023 , Edited by admin on Sat Dec 16 06:35:04 GMT 2023
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DTXSID0044571
Created by
admin on Sat Dec 16 06:35:04 GMT 2023 , Edited by admin on Sat Dec 16 06:35:04 GMT 2023
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210-551-0
Created by
admin on Sat Dec 16 06:35:04 GMT 2023 , Edited by admin on Sat Dec 16 06:35:04 GMT 2023
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SUBSTANCE RECORD