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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)-

Benzenesulfonyl chloride, 5-chloro-2-fluoro-

Clc1ccc(c(c1)S(=O)(=O)Cl)F Request for Quotation
Chemical Name: Benzenesulfonyl chloride, 5-chloro-2-fluoro-
CAS Number: 351003-49-1
Product Number: AG003MMF(AGN-PC-0KKYS0)
Synonyms:
MDL No:
Molecular Formula: C6H3Cl2FO2S
Molecular Weight: 229.0562

Identification/Properties

Properties
MP:
41-44 °C(lit.)
BP:
283.6°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
229.046g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
227.921g/mol
Monoisotopic Mass:
227.921g/mol
Topological Polar Surface Area:
42.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
249
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


5-Chloro-2-fluorobenzenesulfonyl chloride, commonly known as **$name$**, plays a crucial role in chemical synthesis as a versatile reagent. This compound is widely utilized in organic chemistry for the introduction of sulfonyl chloride functional groups into various organic molecules. 
**$name$** acts as an important acylating agent in the creation of amides, sulfonamides, and other related compounds. Its ability to efficiently transfer the sulfonyl chloride group makes it an essential tool in the pharmaceutical industry for the synthesis of diverse drug molecules. Furthermore, this compound is employed in the preparation of sulfonated aromatic compounds, which find applications in materials science and chemical research. 
With its selective reactivity and compatibility with a wide range of substrates, **$name$** enables chemists to perform intricate chemical transformations with high yields and purity. This reagent's role in chemical synthesis highlights its significance in facilitating the creation of complex organic molecules for various industrial and scientific purposes.