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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)-

Benzenemethanesulfonyl chloride, 2,4-dichloro-

Clc1ccc(c(c1)Cl)CS(=O)(=O)Cl Request for Quotation
Chemical Name: Benzenemethanesulfonyl chloride, 2,4-dichloro-
CAS Number: 88691-50-3
Product Number: AG003BKW(AGN-PC-0VN85C)
Synonyms:
MDL No:
Molecular Formula: C7H5Cl3O2S
Molecular Weight: 259.5374

Identification/Properties

Properties
MP:
83-85℃
Form:
Solid
Computed Properties
Molecular Weight:
259.525g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
257.908g/mol
Monoisotopic Mass:
257.908g/mol
Topological Polar Surface Area:
42.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
259
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

GHS Pictogram:
Signal Word:
Danger
UN#:
3261
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2,4-Dichlorophenyl)methanesulfonyl chloride is a versatile chemical reagent commonly used in chemical synthesis for various applications. It serves as a powerful sulfonylating agent, capable of introducing the sulfonyl group onto a wide range of organic molecules. This reagent is especially valued for its ability to selectively react with nucleophilic sites such as amines, alcohols, and thiols, resulting in the formation of sulfonyl derivatives.In organic synthesis, (2,4-Dichlorophenyl)methanesulfonyl chloride plays a crucial role in the protection of sensitive functional groups. By selectively blocking certain reactive sites with the sulfonyl group, chemists can carry out complex multi-step reactions without unwanted side reactions. Additionally, this reagent can be employed in the preparation of sulfonyl fluorides, which are valuable intermediates in pharmaceutical and agrochemical synthesis.Beyond its use as a sulfonylating agent, (2,4-Dichlorophenyl)methanesulfonyl chloride finds applications in the synthesis of sulfonamides, which are important building blocks in medicinal chemistry. The versatility and reactivity of this compound make it a valuable tool for the preparation of a wide range of functionalized organic molecules with diverse applications in the chemical industry.