Benzenesulfenylchloride, 2,4-dinitro-

[ Density]:
1.68g/cm3

[ Boiling Point ]:
430.1ºC at 760 mmHg

[ Melting Point ]:
94-97 °C(lit.)

[ Molecular Formula ]:
C₆H₃ClN₂O₄S

[ Molecular Weight ]:
234.61700

[ Flash Point ]:
213.9ºC

[ Exact Mass ]:
233.95000

[ PSA ]:
116.94000

[ LogP ]:
3.79530

[ Index of Refraction ]:
1.662

[ Storage condition ]:
Store at RT.

Click to get detail MSDS

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C

[ Risk Phrases ]:
34-37

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2930909090

Click to get detail synthetic route

Precursor

DownStream

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Structure-function studies of cholera toxin and its A and B protomers. Modification of tryptophan residues.

J. Biol. Chem. 256(11) , 5481-8, (1981)

The tryptophan residues on cholera toxin and its A and B protomers have been modified by reaction with 2-nitrophenylsulfenyl chloride and 2,4-dinitrophenylsulfenyl chloride. Modification of the trypto...

Involvement and identification of a tryptophanyl residue at the pyruvate binding site of transcarboxylase.

Biochemistry 27(16) , 5978-83, (1988)

Transcarboxylase (TC) from Propionibacterium shermanii consists of a central hexameric 12S subunit to which 6 outer dimeric 5S subunits are attached through 12 biotinyl 1.3S subunits. The enzyme catal...

Studies on the Effect of Remote Substituents on Reactivity: The Rates of Addition of 2, 4-Dinitrobenzenesulfenyl Chloride to Cyclohexenes and Norbornenes (I) 1a. Kwart H and Miller LJ.

J. Am. Chem. Soc. 83(22) , 4552-4559, (1961)

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