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Details

Stereochemistry ACHIRAL
Molecular Formula C13H10O3
Molecular Weight 214.2167
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIPHENYL CARBONATE

SMILES

O=C(OC1=CC=CC=C1)OC2=CC=CC=C2

InChI

InChIKey=ROORDVPLFPIABK-UHFFFAOYSA-N
InChI=1S/C13H10O3/c14-13(15-11-7-3-1-4-8-11)16-12-9-5-2-6-10-12/h1-10H

HIDE SMILES / InChI
Molecular Formula C13H10O3
Molecular Weight 214.2167
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Synthesis of novel aryl(heteroaryl)sulfonyl ureas of possible biological interest.
2010-02-26
Design, synthesis, and analysis of minor groove binder pyrrolepolyamide-2'-deoxyguanosine hybrids.
2010
High-molecular-weight polycarbonates synthesized by enzymatic ROP of a cyclic carbonate as a green process.
2009-10-08
Organic carbonates: experiment and ab initio calculations for prediction of thermochemical properties.
2008-10-23
Dichloro-diphenoxy-methane.
2008-01-04
Catalysis over zinc-incorporated berlinite (ZnAlPO4) of the methoxycarbonylation of 1,6-hexanediamine with dimethyl carbonate to form dimethylhexane-1,6-dicarbamate.
2007-11-07
Nucleofugality of phenyl and methyl carbonates.
2007-10-26
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Substrate specificity of lipases in alkoxycarbonylation reaction: QSAR model development and experimental validation.
2006-06-20
[Preparation and quantitative analysis of methyl phenyl carbonate standard sample].
2006-05
Development and optimization of a method for analysis of the products from the transesterification of dimethyl carbonate and phenol.
2006-01
Effect of metal chlorides on thermal degradation of (waste) polycarbonate.
2006
Method for lipase-catalyzed carbonate synthesis via one- and two-step alkoxycarbonylation reactions.
2003-04-05
[Improved method for determining bisphenol A in polycarbonate products without using dichloromethane].
2003-02
The 13C chemical shift tensor principal values and orientations in dialkyl carbonates and trithiocarbonates.
2002-12
A new heterogeneous catalyst for the oxidative carbonylation of phenol to diphenyl carbonate.
2002-11-21
Patents

Patents

JP1013061A
2
JP2000143960A
1
JP2000178428A
1
JP2000219745A
1
JP2000281817A
1
JP2000355040A
1
JP2001049104A
1
JP2001081179A
1
JP2003503472A
1
JP2003508377A
1
JP2005146048A
1
JP2005146050A
1
JP2005263991A
1
JP2005501115A
1
JP5344927B2
1
JPH01242620A
1
JPH02180925A
1
JPH02215831A
1
JPH02238020A
1
JPH0249025A
1
JPH03168219A
1
JPH041227A
1
JPH041228A
1
JPH041229A
1
JPH04146954A
1
JPH0489824A
1
JPH049357A
1
JPH051145A
1
JPH05310647A
1
JPH058358A
1
JPH06136109A
1
JPH06157739A
1
JPH06228300A
1
JPH0657120A
1
JPH07145107A
1
JPH07207015A
1
JPH07228681A
1
JPH07233314A
1
JPH0726010A
1
JPH08169946A
1
JPH08208824A
1
JPH08208827A
1
JPH08225736A
1
JPH08245774A
1
JPH08325372A
1
JPH0912507A
1
JPH0912511A
1
JPH0912843A
1
JPH09151233A
1
JPH09255772A
1
JPH09278715A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:46:47 GMT 2025
Edited
by admin
on Mon Mar 31 17:46:47 GMT 2025
Record UNII
YWV401IDYN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIPHENYL CARBONATE
HSDB   MI  
Systematic Name English
NSC-37087
Preferred Name English
CARBONIC ACID DIPHENYL ESTER
Systematic Name English
PHENYL CARBONATE
Systematic Name English
DIPHENYL CARBONATE [HSDB]
Common Name English
PHENYL CARBONATE ((PHO)2CO)
Common Name English
DIPHENYL CARBONATE [MI]
Common Name English
Code System Code Type Description
CHEBI
34722
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY
FDA UNII
YWV401IDYN
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY
PUBCHEM
7597
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY
HSDB
5346
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY
EPA CompTox
DTXSID3020540
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY
CAS
102-09-0
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY
MERCK INDEX
m4624
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
203-005-8
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY
NSC
37087
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY
WIKIPEDIA
DIPHENYL CARBONATE
Created by admin on Mon Mar 31 17:46:47 GMT 2025 , Edited by admin on Mon Mar 31 17:46:47 GMT 2025
PRIMARY
NIH
NCATS
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