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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)-

5-Isoquinolinesulfonyl chloride, 1-chloro-

Clc1nccc2c1cccc2S(=O)(=O)Cl Request for Quotation
Chemical Name: 5-Isoquinolinesulfonyl chloride, 1-chloro-
CAS Number: 141519-77-9
Product Number: AG001GIT(AGN-PC-03IKVD)
Synonyms:
MDL No:
Molecular Formula: C9H5Cl2NO2S
Molecular Weight: 262.1125

Identification/Properties

Computed Properties
Molecular Weight:
262.104g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
260.942g/mol
Monoisotopic Mass:
260.942g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
328
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#:
3265
Hazard Statements:
H314
Precautionary Statements:
P260-P280-P303+P361+P353-P301+P330+P331-P304+P340+P310-P305+P351+P338+P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Chloroisoquinoline-5-sulfonyl chloride is a versatile reagent commonly used in chemical synthesis for the introduction of sulfonamide groups onto various organic compounds. This highly reactive compound serves as a sulfonylating agent, enabling the functionalization of a wide range of aromatic substrates. In addition to its sulfonamide-forming capabilities, 1-Chloroisoquinoline-5-sulfonyl chloride is also employed as a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique reactivity and selective sulfonation properties make it a valuable tool in organic synthesis for the creation of diverse molecular structures with potential applications in drug discovery and material science.