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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)-

Cyclopropanemethanesulfonyl chloride

ClS(=O)(=O)CC1CC1 Request for Quotation
Chemical Name: Cyclopropanemethanesulfonyl chloride
CAS Number: 114132-26-2
Product Number: AG000AMY(AGN-PC-0P5UOK)
Synonyms:
MDL No:
Molecular Formula: C4H7ClO2S
Molecular Weight: 154.6152

Identification/Properties

Computed Properties
Molecular Weight:
154.608g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
153.986g/mol
Monoisotopic Mass:
153.986g/mol
Topological Polar Surface Area:
42.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
163
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-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Cyclopropylmethanesulfonyl chloride, also known as CPSCl, is a versatile reagent commonly used in chemical synthesis. This compound is valued for its ability to serve as a sulfonylating agent, allowing for the introduction of the cyclopropylmethanesulfonyl functional group into various organic molecules. In organic synthesis, CPSCl is employed for the preparation of sulfonyl chlorides, which can then be further functionalized to provide access to a diverse array of valuable intermediates and target molecules. This reagent enables chemists to selectively modify molecules, offering control over the regioselectivity and stereochemistry of the resulting products. Furthermore, CPSCl exhibits compatibility with a range of reaction conditions, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and other complex organic compounds.