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Merck
CN

557153

4-(溴甲基)苯磺酰氯

95%

别名:

α-溴-对甲苯磺酰氯

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线性分子式:
BrCH2C6H4SO2Cl
化学文摘社编号:
分子量:
269.54
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

4-(溴甲基)苯磺酰氯, 95%

InChI

1S/C7H6BrClO2S/c8-5-6-1-3-7(4-2-6)12(9,10)11/h1-4H,5H2

SMILES string

ClS(=O)(=O)c1ccc(CBr)cc1

InChI key

QXTQWYZHHMQSQH-UHFFFAOYSA-N

assay

95%

form

solid

mp

71-75 °C (lit.)

functional group

bromo

Quality Level

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

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

存储类别

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

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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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