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Diphenyl carbonate

CAS No.:
102-09-0
Catalog Number:
AG000685
Molecular Formula:
C13H10O3
Molecular Weight:
214.2167
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$19
- +
100g
98%
In Stock USA
United States
$50
- +
500g
98%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG000685
Chemical Name:
Diphenyl carbonate
CAS Number:
102-09-0
Molecular Formula:
C13H10O3
Molecular Weight:
214.2167
MDL Number:
MFCD00003037
IUPAC Name:
diphenyl carbonate
InChI:
InChI=1S/C13H10O3/c14-13(15-11-7-3-1-4-8-11)16-12-9-5-2-6-10-12/h1-10H
InChI Key:
ROORDVPLFPIABK-UHFFFAOYSA-N
SMILES:
O=C(Oc1ccccc1)Oc1ccccc1
EC Number:
203-005-8
UNII:
YWV401IDYN
NSC Number:
37087
Properties
Complexity:
193  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
214.063g/mol
Formal Charge:
0
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
214.22g/mol
Monoisotopic Mass:
214.063g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
35.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.3  
Literature
Title Journal
Effect of the leaving group and solvent combination on the LFER reaction constants. International journal of molecular sciences 20120101
Chemical synthesis of site-specifically 2'-azido-modified RNA and potential applications for bioconjugation and RNA interference. Chembiochem : a European journal of chemical biology 20110103
Synthesis and properties of green sustainable carbonate-type nonionics containing polyoxyethylene chains. Journal of oleo science 20110101
Chemo-enzymatic synthesis and properties of novel optically active cationics containing carbonate linkages. Journal of oleo science 20110101
Chemoenzymatic synthesis and chemical recycling of poly(ester-urethane)s. International journal of molecular sciences 20110101
Synthesis of novel aryl(heteroaryl)sulfonyl ureas of possible biological interest. Molecules (Basel, Switzerland) 20100226
Design, synthesis, and analysis of minor groove binder pyrrolepolyamide-2'-deoxyguanosine hybrids. Journal of nucleic acids 20100101
High-molecular-weight polycarbonates synthesized by enzymatic ROP of a cyclic carbonate as a green process. Macromolecular bioscience 20091008
Organic carbonates: experiment and ab initio calculations for prediction of thermochemical properties. The journal of physical chemistry. A 20081023
Dichloro-diphenoxy-methane. Acta crystallographica. Section E, Structure reports online 20080201
Nucleofugality of phenyl and methyl carbonates. The Journal of organic chemistry 20071026
Catalysis over zinc-incorporated berlinite (ZnAlPO4) of the methoxycarbonylation of 1,6-hexanediamine with dimethyl carbonate to form dimethylhexane-1,6-dicarbamate. Chemistry Central journal 20070101
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. Journal of molecular graphics & modelling 20061101
Substrate specificity of lipases in alkoxycarbonylation reaction: QSAR model development and experimental validation. Biotechnology and bioengineering 20060620
[Preparation and quantitative analysis of methyl phenyl carbonate standard sample]. Se pu = Chinese journal of chromatography 20060501
Development and optimization of a method for analysis of the products from the transesterification of dimethyl carbonate and phenol. Analytical and bioanalytical chemistry 20060101
Effect of metal chlorides on thermal degradation of (waste) polycarbonate. Waste management (New York, N.Y.) 20060101
[Improved method for determining bisphenol A in polycarbonate products without using dichloromethane]. Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan 20030201
Method for lipase-catalyzed carbonate synthesis via one- and two-step alkoxycarbonylation reactions. Biotechnology progress 20030101
The 13C chemical shift tensor principal values and orientations in dialkyl carbonates and trithiocarbonates. Solid state nuclear magnetic resonance 20021201
A new heterogeneous catalyst for the oxidative carbonylation of phenol to diphenyl carbonate. Chemical communications (Cambridge, England) 20021121
Properties