All Photos(3)
Synonym(s):
α-Bromo-p-toluenesulfonyl chloride
Linear Formula:
BrCH2C6H4SO2Cl
CAS Number:
Molecular Weight:
269.54
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
95%
form
solid
mp
71-75 °C (lit.)
SMILES string
ClS(=O)(=O)c1ccc(CBr)cc1
InChI
1S/C7H6BrClO2S/c8-5-6-1-3-7(4-2-6)12(9,10)11/h1-4H,5H2
InChI key
QXTQWYZHHMQSQH-UHFFFAOYSA-N
Related Categories
Application
4-(Bromomethyl)benzenesulfonyl chloride may be used to synthesize:
- 4-bromomethyl-N-(6-methoxy-quinolin-8-yl)-benzenesulfonamide
- benzene-sulfonamide derivatives, which are potent Chemokine Receptor Type 4 (CXCR4) inhibitors
- imidazole derivatives having antifungal activity
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Azizur Rehman et al.
Pakistan journal of pharmaceutical sciences, 32(3), 987-996 (2019-07-07)
Heterocyclic chemistry is an important field of organic chemistry due to therapeutic potential. The minor modification in the structure of poly-functional compounds has great effect on therapeutic ability. In the presented research work, substituted 1,3,4-oxadiazole derivatives, 8a-p, have been synthesized
Pierluigi Teolato et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(8), 2238-2245 (2006-12-13)
Silica nanoparticles (about 15 nm diameters), which contain a derivative of 6-methoxy-8-(p-toluensulfonamido)-quinoline (TSQ) as a Zn(II) fluorescent probe covalently linked to the silica network, were prepared and studied as Zn(II) fluorescent chemosensors. The systems selectively detect Zn(II) ions in water
Suazette Reid Mooring et al.
ChemMedChem, 8(4), 622-632 (2013-03-08)
The interaction of CXCR4 with CXCL12 (SDF-1) plays a critical role in cancer metastasis by facilitating the homing of tumor cells to metastatic sites. Based on our previously published work on CXCR4 antagonists, we have synthesized a series of aryl
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