31283-98-4

Basic information

• Product Name: Benzenesulfonic acid, 2,4-dinitro-, phenyl ester
• Synonyms: Phenyl-2,4-dinitrobenzol-sulfonat;2,4-Dinitro-benzolsulfonsaeure-phenylester;2.4-Dinitrophenylbenzolsulfonat;2,4-Dinitrobenzolsulfonsaeurephenylester
• CAS NO: 31283-98-4
• Molecular Formula: C12H8N2O7S
• Molecular Weight: 324.271
• Mol File: 31283-98-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenesulfonic acid, 2,4-dinitro-, phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonic acid, 2,4-dinitro-, phenyl ester(31283-98-4)
• EPA Substance Registry System: Benzenesulfonic acid, 2,4-dinitro-, phenyl ester(31283-98-4)

Safety Data

• Hazardous Substances Data: 31283-98-4(Hazardous Substances Data)

Upstream product

• 1656-44-6 2,4-dinitrobenzenesulfonyl chloride 
• 108-95-2 phenol 
• 139-02-6 sodium phenoxide 

Downstream Products

• 26289-39-4 S-(2,4-dinitrophenyl)glutathione 
• 1655-62-5 N,S-bis(2,4-dinitrophenyl)cysteine 
• 13059-86-4 2,4-dinitro-N-butylaniline 

Relevant articles and documents

Chemoselective bioconjugation based on modular click chemistry with 4-halocoumarins and aryl sulfonates

We report chemoselective and modular peptide bioconjugation using stoichiometric amounts of 4-halocoumarin and arylsulfonate agents that undergo metal-free C(sp2)-heteroatom bond formation at micromolar concentrations. The underlyingipso-substi

A fluorescence and UV/vis absorption dual-signaling probe with aggregation-induced emission characteristics for specific detection of cysteine

Biological thiols with similar structures, such as glutathione (GSH), N-acetyl-l-cysteine (NAC), homocysteine (Hcy) and cysteine (Cys), play important roles in human physiology and are associated with different diseases. Thus, the discrimination of these

Thiol-activated triplet-triplet annihilation upconversion: Study of the different quenching effect of electron acceptor on the singlet and triplet excited states of bodipy

Thiol-activated triplet-triplet annihilation (TTA) upconversion was studied with two different approaches, i.e., with 2,4-dinitrobenzenenesulfonyl (DNBS)-caged diiodoBodipy triplet photosensitizers (perylene as the triplet acceptor/emitter of the upconver