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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)-

Ethanone, 2-chloro-1-(1-chlorocyclopropyl)-

ClCC(=O)C1(Cl)CC1 Request for Quotation
Chemical Name: Ethanone, 2-chloro-1-(1-chlorocyclopropyl)-
CAS Number: 120983-72-4
Product Number: AG0074G2(AGN-PC-0NF9FC)
Synonyms:
MDL No:
Molecular Formula: C5H6Cl2O
Molecular Weight: 153.0065

Identification/Properties

Computed Properties
Molecular Weight:
153.002g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
151.98g/mol
Monoisotopic Mass:
151.98g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
118
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


2-Chloro-1-(1-chlorocyclopropyl)ethanone, also known as $name$, is a versatile compound that plays a key role in chemical synthesis processes. This specific compound is frequently utilized as a crucial building block in the creation of various organic molecules due to its unique structure and reactivity.In chemical synthesis, 2-Chloro-1-(1-chlorocyclopropyl)ethanone serves as a valuable intermediate for the preparation of complex compounds such as pharmaceuticals, agrochemicals, and organic materials. Its cyclopropyl ring imparts structural rigidity and provides an opportunity for stereochemical control during reactions.Moreover, the presence of the chloro groups in the molecule facilitates further derivatization through substitution or elimination reactions, enabling chemists to tailor the compound for specific applications. This compound's ability to participate in diverse chemical transformations makes it a significant tool in the toolkit of synthetic chemists for designing and constructing novel molecular structures with desired properties.