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Merck
모든 사진(1)

문서

532711

Sigma-Aldrich

2-Fluorobenzenesulfonyl chloride

97%

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About This Item

Linear Formula:
FC6H4SO2Cl
CAS Number:
Molecular Weight:
194.61
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

97%

refractive index

n20/D 1.537 (lit.)

bp

246-247 °C (lit.)

mp

27-30 °C (lit.)

density

1.47 g/mL at 25 °C (lit.)

SMILES string

Fc1ccccc1S(Cl)(=O)=O

InChI

1S/C6H4ClFO2S/c7-11(9,10)6-4-2-1-3-5(6)8/h1-4H

InChI key

ZSZKAQCISWFDCQ-UHFFFAOYSA-N

일반 설명

2-Fluorobenzenesulfonyl chloride, also known as o-fluorobenzenesulfonyl chloride, is a flurinated arylsulfonyl chloride. It can be prepared from o-benzenedisulfonyl fluoride.

애플리케이션

2-Fluorobenzenesulfonyl chloride may be used in the preparation of the following furan derivatives:
  • 2-(2-fluorophenyl)benzofuran
  • 2-butyl-5-(2-fluorophenyl)furan
  • 2-(2-fluorophenyl)-3,6-dimethyl-4,5,6,7-tetrahydrobenzofuran

It may also be used to prepare:
  • 2-fluorobenzenesulfonamide
  • methyl 2-{[(2-fluorophenyl)sulfonyl]amino}-5,6,7,8-tetrahydro-1-naphthalenecarboxylate
  • potassium fluorobenzene-2-sulfonate
  • 1-(2-bromobenzyl)-2-(2-fluorophenyl)pyrrole

픽토그램

Corrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

230.0 °F - closed cup

Flash Point (°C)

110 °C - closed cup

개인 보호 장비

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


시험 성적서(COA)

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문서 라이브러리 방문

Discovery and optimization of anthranilic acid sulfonamides as inhibitors of methionine aminopeptidase-2: a structural basis for the reduction of albumin binding.
Sheppard GS, et al.
Journal of Medicinal Chemistry, 49(13), 3832-3849 (2006)
Water-Soluble Phosphines. 6.1 Tailor-Made Syntheses of Chiral Secondary and Tertiary Phosphines with Sulfonated Aromatic Substituents: Structural and Quantum Chemical Studies.
Bitterer F, et al.
Inorganic Chemistry, 35(14), 4103-4113 (1996)
Regiocontroled Palladium?Catalysed Direct Arylation at Carbon C2 of Benzofurans using Benzenesulfonyl Chlorides as the Coupling Partners.
Loukotova L, et al.
ChemCatChem, 6(5), 1303-1309 (2014)
Benzenesulfonyl Chlorides: Alternative Coupling Partners for Regiocontrolled Palladium-Catalyzed Direct Desulfitative 5-Arylation of Furans.
Beladhria A, et al.
Synthesis, 46(18), 2515-2523 (2014)
Palladium-Catalyzed Iterative C- H Bond Arylations: Synthesis of Medium-Size Heterocycles with a Bridgehead Nitrogen Atom.
Hagui W, et al.
ChemCatChem, 7(21), 3544-3554 (2015)

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