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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, 2,3,4-trichloro-

Clc1ccc(c(c1Cl)Cl)S(=O)(=O)Cl Request for Quotation
Chemical Name: Benzenesulfonyl chloride, 2,3,4-trichloro-
CAS Number: 34732-09-7
Product Number: AG003FE4(AGN-PC-0JKPBU)
Synonyms:
MDL No:
Molecular Formula: C6H2Cl4O2S
Molecular Weight: 279.9559

Identification/Properties

Properties
MP:
62-66℃
Form:
Solid
Computed Properties
Molecular Weight:
279.94g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
279.85g/mol
Monoisotopic Mass:
277.853g/mol
Topological Polar Surface Area:
42.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
273
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


2,3,4-Trichlorobenzene-1-sulfonyl chloride is a versatile chemical reagent widely utilized in chemical synthesis due to its unique properties. It serves as a valuable acylating agent in organic reactions, specifically in the formation of amides and esters. This compound is highly reactive and selective, allowing for precise control over the acylation process. Additionally, 2,3,4-Trichlorobenzene-1-sulfonyl chloride is commonly employed in the synthesis of pharmaceutical intermediates and agrochemicals, highlighting its importance in the production of valuable compounds with diverse applications. Its ability to functionalize a wide range of substrates makes it a crucial tool in the arsenal of synthetic chemists looking to create complex molecules efficiently and effectively.