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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)-

Cyclopropanesulfonyl chloride, 1-(2-propen-1-yl)-

C=CCC1(CC1)S(=O)(=O)Cl Request for Quotation
Chemical Name: Cyclopropanesulfonyl chloride, 1-(2-propen-1-yl)-
CAS Number: 923032-59-1
Product Number: AG00GRLW(AGN-PC-0723XQ)
Synonyms:
MDL No:
Molecular Formula: C6H9ClO2S
Molecular Weight: 180.6525

Identification/Properties

Computed Properties
Molecular Weight:
180.646g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
180.001g/mol
Monoisotopic Mass:
180.001g/mol
Topological Polar Surface Area:
42.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
233
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile compound that plays a crucial role in chemical synthesis as a key reagent. Specifically, it is commonly utilized in the construction of diverse molecular structures through various synthetic pathways. Its reactivity as a sulfonyl chloride derivative makes it an essential building block in the preparation of complex organic molecules.In chemical synthesis, $name$ can serve as a valuable tool in the installation of functional groups or the modification of existing functionalities within a molecule. By participating in a range of reactions, such as nucleophilic substitution or rearrangement processes, it enables chemists to access novel intermediates and target compounds with significant synthetic utility.Furthermore, the unique properties of $name$ make it particularly advantageous for the creation of challenging ring systems or the formation of highly strained molecular frameworks. Its incorporation into strategic synthetic sequences has been demonstrated to facilitate the efficient assembly of intricate molecular architectures with tailored properties for a variety of applications.Overall, the application of Cyclopropanesulfonyl chloride, 1-(2-propen-1-yl)- in chemical synthesis underscores its significance as a versatile reagent for the construction of complex organic molecules with enhanced structural diversity and functionality.