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Details

Stereochemistry ACHIRAL
Molecular Formula C14H10O3
Molecular Weight 226.2274
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZOIC ANHYDRIDE

SMILES

O=C(OC(=O)C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=CHIHQLCVLOXUJW-UHFFFAOYSA-N
InChI=1S/C14H10O3/c15-13(11-7-3-1-4-8-11)17-14(16)12-9-5-2-6-10-12/h1-10H

HIDE SMILES / InChI

Approval Year

2018
436
PubMed

PubMed

TitleDatePubMed
An effective use of benzoic anhydride and its derivatives for the synthesis of carboxylic esters and lactones: a powerful and convenient mixed anhydride method promoted by basic catalysts.
2004 Mar 19
Derivatization for LC-electrospray ionization-MS: a tool for improving reversed-phase separation and ESI responses of bases, ribosides, and intact nucleotides.
2004 May 15
Synthesis of lactones using substituted benzoic anhydride as a coupling reagent.
2007
In vitro screening of anti-lice activity of Pongamia pinnata leaves.
2009 Dec
2,3-Diamino-pyridinium benzoate benzoic acid solvate.
2010 Jan 30
Patents

Patents

03931281
1
03932661
3
03968140
1
03985880
2
03994956
1
04198412
1
04202975
3
04347370
3
04374923
1
04426388
2
04522822
2
04666907
3
04845083
3
05010060
3
05095015
1
05378713
1
05399720
1
05541313
1
05872255
1
05889024
2
06013650
2
07199138
1
07507740
3
07595425
1
07741326
2
08598192
3
08822456
5
JP2005533893A
4
JPH0899982A
1
JPH0940608A
1
JPS5738804A
1
JPS58129054A
1
JPS62101415A
1
Name Type Language
BENZOIC ANHYDRIDE
MI  
Systematic Name English
BENZOYL ANHYDRIDE
Common Name English
NSC-37116
Code English
BENZOYLBENZOATE
Systematic Name English
BENZOIC ANHYDRIDE [MI]
Common Name English
BENZOYL BENZOATE
Systematic Name English
Code System Code Type Description
DAILYMED
9K7X34FOV2
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
MESH
C102988
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
EVMPD
SUB13015MIG
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
ECHA (EC/EINECS)
202-291-1
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
CAS
93-97-0
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
MERCK INDEX
m2364
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY Merck Index
PUBCHEM
7167
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
EPA CompTox
DTXSID1029122
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
RXCUI
1998050
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
SMS_ID
100000077157
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
WIKIPEDIA
Benzoic anhydride
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
FDA UNII
9K7X34FOV2
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
CHEBI
38815
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
NSC
37116
Created by admin on Fri Dec 15 18:52:46 UTC 2023 , Edited by admin on Fri Dec 15 18:52:46 UTC 2023
PRIMARY
SUBSTANCE RECORD
Structure of BENZOIC ANHYDRIDE
NIH
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