Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H12O2 |
Molecular Weight | 152.1904 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=CC=C(O)C(O)=C1
InChI
InChIKey=WYVMDJWLFVQZAL-UHFFFAOYSA-N
InChI=1S/C9H12O2/c1-6(2)7-3-4-8(10)9(11)5-7/h3-6,10-11H,1-2H3
Molecular Formula | C9H12O2 |
Molecular Weight | 152.1904 |
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 |
---|---|---|
Molecular mechanisms controlling the rate and specificity of catechol O-methylation by human soluble catechol O-methyltransferase. | 2001 Feb |
|
ipso-substitution: a general biochemical and biodegradation mechanism to cleave alpha-quaternary alkylphenols and bisphenol A. | 2007 Sep |
|
Evaluation of skin diseases and disorders in photographers. | 2009 Aug |
|
Chemical leucoderma: Indian scenario, prognosis, and treatment. | 2010 Jul-Sep |
|
Isolation and characterization of 4-tert-butylphenol-utilizing Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment. | 2010 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:26:44 GMT 2023
by
admin
on
Fri Dec 15 15:26:44 GMT 2023
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Record UNII |
SE856V0X6N
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Record Status |
Validated (UNII)
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Record Version |
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C013074
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DTXSID20175643
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SE856V0X6N
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