108669
4-Bromobenzenesulfonyl chloride
98%
Synonym(s):
p-Bromobenzenesulfonyl chloride, Brosyl chloride
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About This Item
Linear Formula:
BrC6H4SO2Cl
CAS Number:
Molecular Weight:
255.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-683-2
Beilstein/REAXYS Number:
743518
MDL number:
Assay:
98%
InChI key
KMMHZIBWCXYAAH-UHFFFAOYSA-N
InChI
1S/C6H4BrClO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H
SMILES string
ClS(=O)(=O)c1ccc(Br)cc1
assay
98%
bp
153 °C/15 mmHg (lit.)
Quality Level
functional group
bromo
Related Categories
Application
4-Bromobenzenesulfonyl chloride was used as activating agent in the synthesis of oligodeoxyribo- and oligoribo- nucleotides in solution. It was used in the synthesis of 4-(N-allylsulfamoyl)phenylboronic acid.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
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
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Xiaobao Li et al.
Analytical biochemistry, 372(2), 227-236 (2007-10-20)
Two new types of boronate affinity solid phases were synthesized and characterized. The materials were prepared by silylation of porous silica gel with monochlorosilane derivatives containing synthetic sulfonyl- and sulfonamide-substituted phenylboronic acids. The new solid phases were evaluated for boronate
Phosphotriester approach to the synthesis of oligonucleotides: a reappraisal.
Reese CB and Pei-Zhuo Z.
Journal of the Chemical Society. Perkin Transactions 1, 1(19), 2291-2301 (1993)
Tsurng-Juhn Huang et al.
European journal of medicinal chemistry, 90, 428-435 (2014-12-03)
Hepatitis B virus (HBV) is a causative reagent that frequently causes progressive liver diseases, leading to the development of acute, chronic hepatitis, cirrhosis, and eventually hepatocellular carcinoma (HCC). Despite several antiviral drugs including interferon-α and nucleotide derivatives are approved for
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