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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)-

6-Benzothiazolesulfonyl chloride

ClS(=O)(=O)c1ccc2c(c1)scn2 Request for Quotation
Chemical Name: 6-Benzothiazolesulfonyl chloride
CAS Number: 181124-40-3
Product Number: AG0022P0(AGN-PC-0KL7CJ)
Synonyms:
MDL No:
Molecular Formula: C7H4ClNO2S2
Molecular Weight: 233.6952

Identification/Properties

Computed Properties
Molecular Weight:
233.684g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
232.937g/mol
Monoisotopic Mass:
232.937g/mol
Topological Polar Surface Area:
83.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
287
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#:
1759
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


When utilized in chemical synthesis, 1,3-Benzothiazole-6-sulfonyl chloride serves as a valuable reagent for introducing the sulfonyl chloride functional group into organic molecules. This compound is instrumental in various organic reactions such as nucleophilic substitution and condensation reactions, where the sulfonyl chloride moiety can act as a versatile protecting group or a reactive electrophile. By exploiting the reactivity of 1,3-Benzothiazole-6-sulfonyl chloride, chemists can efficiently modify and functionalize organic compounds to create novel structures and tailor properties for specific applications in the pharmaceutical, agrochemical, and materials science industries.