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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)-

Cyclopropanecarbonyl chloride, 2-phenyl-, (1R,2R)-rel-

ClC(=O)[C@@H]1C[C@H]1c1ccccc1 Request for Quotation
Chemical Name: Cyclopropanecarbonyl chloride, 2-phenyl-, (1R,2R)-rel-
CAS Number: 939-87-7
Product Number: AG003UWR(AGN-PC-0W3MNU)
Synonyms:
MDL No:
Molecular Formula: C10H9ClO
Molecular Weight: 180.6309

Identification/Properties

Computed Properties
Molecular Weight:
180.631g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
180.034g/mol
Monoisotopic Mass:
180.034g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
184
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Trans-2-phenylcyclopropanecarbonyl chloride, also known as $name$, is a versatile chemical compound used in a variety of applications within chemical synthesis. This compound is valued for its ability to act as an acylating agent in reactions, providing a valuable tool for the creation of complex organic molecules. Specifically, $name$ is often utilized in the preparation of pharmaceutical compounds, agrochemicals, and advanced materials due to its unique reactivity and role in forming key chemical bonds. Its use in organic synthesis allows chemists to introduce the phenylcyclopropane moiety in a controlled and efficient manner, enabling the synthesis of compounds with specific structural features and desired properties. By offering a way to functionalize molecules with precision, $name$ plays a crucial role in the development of novel chemicals and materials with diverse applications across various industries.