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Chemical structure of p-Nitrobenzyl mesylate

GC44663

p-Nitrobenzyl mesylate

Also known as (4-nitrophenyl)methyl methanesulfonate

p-Nitrobenzyl mesylate (PNBM) is an alkylating agent used to identify direct kinase substrates· The alkylation mechanism of p-Nitrobenzyl mesylate is to alkylate the phosphorothioate site to form a phosphorothioate epitope

ChemicalCAS39628-94-9MW231.2FormulaC8H9NO5S
CAS number
39628-94-9
Molecular weight
231.2
Formula
C8H9NO5S
Solubility
100mM in DMSO
InChIKey
QZIYKAFPHRTIAI-UHFFFAOYSA-N
Catalogue number
GC44663
Brand
GLPBIO
Computed properties PubChem CID 18924794 · XLogP 1 · TPSA 97.6 Ų · H-bond donors 0
XLogP
1
TPSA
97.6 Ų
H-bond donors
0
H-bond acceptors
5
Rotatable bonds
3
Heavy atoms
15

SMILES CS(=O)(=O)OCC1=CC=C(C=C1)[N+](=O)[O-]

Computed descriptors from PubChem (CID 18924794), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

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