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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)-

3-Furansulfonyl chloride, 2,5-dimethyl-

Cc1oc(c(c1)S(=O)(=O)Cl)C Request for Quotation
Chemical Name: 3-Furansulfonyl chloride, 2,5-dimethyl-
CAS Number: 166964-26-7
Product Number: AG001X1J(AGN-PC-0KL79N)
Synonyms:
MDL No:
Molecular Formula: C6H7ClO3S
Molecular Weight: 194.6360

Identification/Properties

Computed Properties
Molecular Weight:
194.629g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
193.98g/mol
Monoisotopic Mass:
193.98g/mol
Topological Polar Surface Area:
55.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
231
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Dimethylfuran-3-sulfonyl chloride is a versatile chemical reagent used extensively in organic synthesis. Its application in chemical reactions is particularly noteworthy in the synthesis of various pharmaceutical compounds and natural products. This compound serves as an important building block in the creation of complex molecules due to its ability to function as both a sulfonyl chloride and a furan ring system. In chemical synthesis, 2,5-Dimethylfuran-3-sulfonyl chloride is commonly employed for the introduction of the sulfonyl chloride functional group into target molecules, enabling the formation of key intermediates. Furthermore, its unique structure allows for selective and efficient derivatization processes, making it an indispensable tool in the development of new materials and bioactive compounds.