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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2,3,5-Trifluorobenzenesulfonyl chloride, JRD, 97%

Fc1cc(F)c(c(c1)S(=O)(=O)Cl)F Request for Quotation
Chemical Name: 2,3,5-Trifluorobenzenesulfonyl chloride, JRD, 97%
CAS Number: 914636-99-0
Product Number: AG00H1S8(AGN-PC-0WAONR)
Synonyms:
MDL No:
Molecular Formula: C6H2ClF3O2S
Molecular Weight: 230.5921

Identification/Properties

Computed Properties
Molecular Weight:
230.585g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
229.942g/mol
Monoisotopic Mass:
229.942g/mol
Topological Polar Surface Area:
42.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
276
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3,5-Trifluorobenzenesulphonyl chloride is a versatile chemical compound that finds wide application in chemical synthesis. Specifically, it is commonly utilized as a sulfonylating agent in organic reactions. By introducing the sulfonyl chloride group to various organic molecules, this reagent enables the formation of new carbon-sulfur bonds. This can be crucial in the synthesis of complex organic compounds, such as pharmaceuticals, agrochemicals, and materials. Additionally, 2,3,5-Trifluorobenzenesulphonyl chloride is valued for its ability to act as a protecting group for alcohols and amines, safeguarding these functional groups during synthetic transformations and facilitating selective reactions. Its compatibility with a wide range of substrates and its high reactivity make it a valuable tool in the toolkit of synthetic chemists.