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Merck
모든 사진(1)

주요 문서

545716

Sigma-Aldrich

3-Bromobenzenesulfonyl chloride

96%

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About This Item

Linear Formula:
BrC6H4SO2Cl
CAS Number:
Molecular Weight:
255.52
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

96%

refractive index

n20/D 1.593 (lit.)

bp

90-91 °C/0.5 mmHg (lit.)

mp

30-33 °C

density

1.773 g/mL at 25 °C (lit.)

작용기

bromo

SMILES string

ClS(=O)(=O)c1cccc(Br)c1

InChI

1S/C6H4BrClO2S/c7-5-2-1-3-6(4-5)11(8,9)10/h1-4H

InChI key

PJGOLCXVWIYXRQ-UHFFFAOYSA-N

일반 설명

3-Bromobenzenesulfonyl chloride is an aryl sulfonyl chloride derivative. It participates in the synthesis of N-sulfonylanthranilic acid derivatives and potent P1′ benzenesulfonyl azacyclic urea human immunodeficiency virus (HIV) protease inhibitors.

애플리케이션

3-Bromobenzenesulfonyl chloride may be used in the preparation of:
  • 2-(3-bromophenyl)-5-n-butylfuran
  • 2-(3-bromophenyl)-3,6-dimethyl-4,5,6,7-tetrahydrobenzofuran
  • 3-bromo-4-(3-bromophenyl)thiophene
  • 2,5-bis(3-bromophenyl)-1-methylpyrrole

픽토그램

Corrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Pd?Catalysed Direct Arylation of Heteroaromatics Using (Poly) halobenzenesulfonyl Chlorides as Coupling Partners: One Step Access to (Poly) halo?Substituted Bi (hetero) aryls.
Skhiri A, et al.
European Journal of Organic Chemistry, 2015(20), 4428-4436 (2015)
Peggy P Huang et al.
Bioorganic & medicinal chemistry letters, 14(15), 4075-4078 (2004-07-01)
A series of novel azacyclic urea HIV protease inhibitors bearing a benzenesulfonamide group at P1' were synthesized utilizing a parallel synthesis method. Structural studies of early analogs bound in the enzyme active site were used to design more potent inhibitors.
Zheng Yin et al.
Journal of medicinal chemistry, 52(24), 7934-7937 (2009-12-18)
A novel class of compounds containing N-sulfonylanthranilic acid was found to specifically inhibit dengue viral polymerase. The structural requirements for inhibition and a preliminary structure-activity relationship are described. A UV cross-linking experiment was used to map the allosteric binding site

문서

Aryl sulfonyl chloride derivatives are frequently used in parallel synthesis to synthesize sulfonamides and sulfonate linkages.

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