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959-22-8 | 4-Nitrophenyl benzoate, 97%
CAS No: 959-22-8 Catalog No: AG003LVV MDL No:MFCD00135494
Product Description
Catalog Number:
AG003LVV
Chemical Name:
4-Nitrophenyl benzoate, 97%
CAS Number:
959-22-8
MDL Number:
MFCD00135494
IUPAC Name:
(4-nitrophenyl) benzoate
InChI:
InChI=1S/C13H9NO4/c15-13(10-4-2-1-3-5-10)18-12-8-6-11(7-9-12)14(16)17/h1-9H
InChI Key:
GMKZBFFLCONHDE-UHFFFAOYSA-N
EC Number:
917-588-8
NSC Number:
408882
Properties
Complexity:
299
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
243.053g/mol
Formal Charge:
0
Heavy Atom Count:
18
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
243.218g/mol
Monoisotopic Mass:
243.053g/mol
Rotatable Bond Count:
3
Topological Polar Surface Area:
72.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.4
Literature
| Title | Journal |
|---|---|
| The catalytic serine of meta-cleavage product hydrolases is activated differently for C-O bond cleavage than for C-C bond cleavage. | Biochemistry 20120724 |
| Promiscuous esterase activities of the C-C hydrolases from Dyella ginsengisoli. | Biotechnology letters 20120601 |
| Nucleophilic attack of salicylhydroxamate ion at C=O and P=O centers in cationic micellar media. | The journal of physical chemistry. B 20101223 |
| Effects on the reactivity by changing the electrophilic center from C==O to C==S: contrasting reactivity of hydroxide, p-chlorophenoxide, and butan-2,3-dione monoximate in DMSO/H2O mixtures. | Chemistry (Weinheim an der Bergstrasse, Germany) 20090101 |
| Modification of both the electrophilic center and substituents on the nonleaving group in pyridinolysis of O-4-nitrophenyl benzoate and thionobenzoates. | The Journal of organic chemistry 20061124 |
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