Skip to Content
Merck
CN

142956

2,4-Dinitrobenzenesulfonyl chloride

97%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
(O2N)2C6H3SO2Cl
CAS Number:
Molecular Weight:
266.62
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2147583
Assay:
97%
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


assay

97%

form

solid

mp

101-103 °C (lit.)

functional group

nitro

SMILES string

[O-][N+](=O)c1ccc(c(c1)[N+]([O-])=O)S(Cl)(=O)=O

InChI

1S/C6H3ClN2O6S/c7-16(14,15)6-2-1-4(8(10)11)3-5(6)9(12)13/h1-3H

InChI key

SSFSNKZUKDBPIT-UHFFFAOYSA-N

General description

2,4-Dinitrobenzenesulfonyl chloride causes the sulfonation of glycosylamines to yield N-glycosyl-2,4-dinitrobenzenesulfonamides.
May contain up to 3.5% benzene

Application

2,4-Dinitrobenzenesulfonyl chloride was used to protect primary amines. It was used as starting reagent in the synthesis of tert-butyl 2-[(2,4-dinitrophenyl) sulfonyl]aminoacetate.


pictograms

Health hazardCorrosion

signalword

Danger

Hazard Classifications

Carc. 1A - Eye Dam. 1 - Muta. 1B - Skin Corr. 1B - STOT RE 2

target_organs

Blood

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

危险化学品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



Vishwanath Gaitonde et al.
Journal of carbohydrate chemistry, 31(4-6), 353-370 (2013-01-26)
The N-glycosyl-2,4-dinitrobenzenesulfonamides were accessed via benzoyl-protected β-glycosyl azides. The azides were reduced with Adams' catalyst to the corresponding amines. The glycosylamines were sulfonated with 2,4-dinitrobenzenesulfonyl chloride to form N-glycosyl-2,4-dinitrobenzenesulfonamides in moderate yields. β-Glycosyl amides were then prepared in 67 -
Rachel J Ball et al.
Artificial DNA, PNA & XNA, 1(1), 27-35 (2011-06-21)
Halogen-labelled peptide organic acid (HPOA) monomers have been synthesised and incorporated into sequence-specific peptide nucleic acid (PNA) probes. Three different types of probe have been prepared; the unmodified PNA probe, the PNA probe with a mass marker, and the PNA



Global Trade Item Number

SKUGTIN
142956-5G04061838734556
142956-25G04061838734549