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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)-

Cyclopropanesulfonic acid, butyl ester

CCCCOS(=O)(=O)C1CC1 Request for Quotation
Chemical Name: Cyclopropanesulfonic acid, butyl ester
CAS Number: 83635-12-5
Product Number: AG004TSK(AGN-PC-0N4W2Z)
Synonyms:
MDL No:
Molecular Formula: C7H14O3S
Molecular Weight: 178.2493

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Butyl cyclopropanesulfonate is a versatile chemical compound widely used in organic synthesis as a reactive intermediate. This compound plays a crucial role in various chemical reactions due to its ability to easily undergo substitution reactions with nucleophiles, making it a valuable building block in the creation of complex organic molecules. One common application of butyl cyclopropanesulfonate is its use as a leaving group in nucleophilic substitution reactions, where it can be replaced by a nucleophile to generate new carbon-carbon or carbon-heteroatom bonds. Additionally, this compound is also utilized in the synthesis of biologically active compounds, pharmaceuticals, and agrochemicals, highlighting its significance in the field of medicinal chemistry and drug discovery.