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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)-

4-pyridin-2-yloxybenzenesulfonyl chloride;hydrochloride

ClS(=O)(=O)c1ccc(cc1)Oc1ccccn1.Cl Request for Quotation
Chemical Name: 4-pyridin-2-yloxybenzenesulfonyl chloride;hydrochloride
CAS Number: 1170110-04-9
Product Number: AG000DJH(AGN-PC-01NOSG)
Synonyms:
MDL No:
Molecular Formula: C11H9Cl2NO3S
Molecular Weight: 306.1651

Identification/Properties

Computed Properties
Molecular Weight:
306.157g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
304.968g/mol
Monoisotopic Mass:
304.968g/mol
Topological Polar Surface Area:
64.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
333
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
3261
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


4-(Pyridin-2-yloxy)benzene-1-sulfonyl chloride hydrochloride is a versatile chemical reagent commonly utilized in chemical synthesis reactions. Its primary application lies in the field of organic chemistry, particularly in the preparation of various functionalized molecules and pharmaceutical intermediates.One key function of 4-(Pyridin-2-yloxy)benzene-1-sulfonyl chloride hydrochloride is its ability to serve as a sulfonyl chloride derivative, which can undergo nucleophilic substitution reactions with a wide range of nucleophiles. This characteristic makes it a valuable building block in the synthesis of sulfonamides, sulfones, and other sulfonate compounds.Furthermore, the presence of the pyridine moiety in its structure imparts unique reactivity, allowing for selective functionalization at the aromatic ring. This enables chemists to introduce specific substituents or structural motifs in a controlled manner, facilitating the design and synthesis of novel organic molecules with tailored properties.Overall, the strategic incorporation of 4-(Pyridin-2-yloxy)benzene-1-sulfonyl chloride hydrochloride in chemical synthesis offers researchers a powerful tool for the efficient construction of complex molecular architectures and the exploration of new chemical space in drug discovery and material science applications.