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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)-

Cyclopentanecarboxylic acid, 1-(4-bromophenyl)-

OC(=O)C1(CCCC1)c1ccc(cc1)Br Request for Quotation
Chemical Name: Cyclopentanecarboxylic acid, 1-(4-bromophenyl)-
CAS Number: 143328-24-9
Product Number: AG009B3G(AGN-PC-0JWM2Y)
Synonyms:
MDL No: MFCD00455267
Molecular Formula: C12H13BrO2
Molecular Weight: 269.1344

Identification/Properties

Computed Properties
Molecular Weight:
269.138g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
268.01g/mol
Monoisotopic Mass:
268.01g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
238
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:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Bromophenyl)cyclopentane-1-carboxylic acid is a versatile compound widely utilized in chemical synthesis due to its unique structure and reactivity. As a key building block in organic chemistry, this molecule serves as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its cyclopentane ring imparts rigidity and stereochemical control, making it particularly useful in the synthesis of complex molecules with defined spatial arrangements. With its bromophenyl moiety, this compound can participate in diverse carbon-carbon bond forming reactions, enabling the construction of diverse molecular architectures. In addition, the carboxylic acid group provides a handle for further functionalization, facilitating the incorporation of additional structural motifs or bioactive elements. In summary, 1-(4-Bromophenyl)cyclopentane-1-carboxylic acid plays a crucial role in the development of novel compounds with potential applications in various fields of chemistry.