Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H5O.K |
Molecular Weight | 132.2016 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[K+].[O-]C1=CC=CC=C1
InChI
InChIKey=ZGJADVGJIVEEGF-UHFFFAOYSA-M
InChI=1S/C6H6O.K/c7-6-4-2-1-3-5-6;/h1-5,7H;/q;+1/p-1
Molecular Formula | K |
Molecular Weight | 39.0983 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C6H5O |
Molecular Weight | 93.1033 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
PubMed
Title | Date | PubMed |
---|---|---|
Synthesis of indole-3-carboxylic acid derivatives by Pd(0)-catalyzed intramolecular alpha-arylation of beta-(2-iodoanilino) esters. | 2008 Mar 21 |
|
Effects of charge separation, effective concentration, and aggregate formation on the phase transfer catalyzed alkylation of phenol. | 2012 Aug 15 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 20:01:52 GMT 2023
by
admin
on
Sat Dec 16 20:01:52 GMT 2023
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Record UNII |
9CQ00ODF3U
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Record Status |
Validated (UNII)
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Record Version |
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DTXSID30881405
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9CQ00ODF3U
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202-877-7
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23670670
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m9048
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admin on Sat Dec 16 20:01:53 GMT 2023 , Edited by admin on Sat Dec 16 20:01:53 GMT 2023
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100-67-4
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admin on Sat Dec 16 20:01:53 GMT 2023 , Edited by admin on Sat Dec 16 20:01:53 GMT 2023
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |