U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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

Molecular Formula C14H10O3
Molecular Weight 226.2274
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Stable, dispersible surface-enhanced Raman scattering substrate capable of detecting molecules bound to silica-immobilized ligands.
2010-11
Selective monoacylation of ferrocene with bulky acylating agents over mesoporous sieve AlKIT-5.
2010-07-12
2,3-Diamino-pyridinium benzoate benzoic acid solvate.
2010-01-30
Crusted (Norwegian) scabies following systemic and topical corticosteroid therapy.
2010-01
Merging nucleophilic and hydrogen bonding catalysis: an anion binding approach to the kinetic resolution of amines.
2009-12-02
In vitro screening of anti-lice activity of Pongamia pinnata leaves.
2009-12
High burden of impetigo and scabies in a tropical country.
2009-06-23
Total synthesis of 2-hydroxytetracosanolide and 2-hydroxy-24-oxooctacosanolide by using an effective lactonization.
2008-02-01
Specific anion binding to sulfobetaine micelles and kinetics of nucleophilic reactions.
2007-08-23
Synthesis of lactones using substituted benzoic anhydride as a coupling reagent.
2007
Nucleophilic acyl substitutions of anhydrides with protic nucleophiles catalyzed by amphoteric, oxomolybdenum species.
2005-02-18
Derivatization for LC-electrospray ionization-MS: a tool for improving reversed-phase separation and ESI responses of bases, ribosides, and intact nucleotides.
2004-05-15
Porphyrin ring contraction: a one-pot reaction leading to divalent corroles.
2004-05-07
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.
2004-03-19
Desymmetrization of meso-hydrobenzoin using chiral, nucleophilic phosphine catalysts.
2004-02-20
Demodex abscesses: clinical and therapeutic challenges.
2003-11
The ultrasonically induced reaction of benzoyl chloride with nitrobenzene: an unexpected sonochemical effect and a possible mechanism.
2002-10
Liquid chromatographic determination of ampicillin residues in porcine muscle tissue by a multipenicillin analytical method: European Collaborative Study.
2002-08-16
A capillary zone electrophoresis method for determining N-acetylneuraminic acid in glycoproteins and blood sera.
2002-04
Preparative route to glucuronyl donors bearing temporary protecting group at O-3 via 6,3-lactonisation by Bz(2)O or Piv(2)O.
2001-12-07
Efficient preparation of (R)-alpha-monobenzoyl glycerol by lipase catalyzed asymmetric esterification: optimization and operation in packed bed reactor.
2001-06-20
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:23:36 GMT 2025
Edited
by admin
on Mon Mar 31 19:23:36 GMT 2025
Record UNII
9K7X34FOV2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-37116
Preferred Name English
BENZOIC ANHYDRIDE
MI  
Systematic Name English
BENZOYL ANHYDRIDE
Common Name 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 Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
MESH
C102988
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
EVMPD
SUB13015MIG
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-291-1
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
CAS
93-97-0
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
MERCK INDEX
m2364
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY Merck Index
PUBCHEM
7167
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
EPA CompTox
DTXSID1029122
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
RXCUI
1998050
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
SMS_ID
100000077157
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
WIKIPEDIA
Benzoic anhydride
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
FDA UNII
9K7X34FOV2
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
CHEBI
38815
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY
NSC
37116
Created by admin on Mon Mar 31 19:23:36 GMT 2025 , Edited by admin on Mon Mar 31 19:23:36 GMT 2025
PRIMARY