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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)-

2-(3-bromophenyl)cyclopropane-1-carboxylic acid

OC(=O)C1CC1c1cccc(c1)Br Request for Quotation
Chemical Name: 2-(3-bromophenyl)cyclopropane-1-carboxylic acid
CAS Number: 91445-84-0
Product Number: AG00H30N(AGN-PC-03R9ZV)
Synonyms:
MDL No:
Molecular Formula: C10H9BrO2
Molecular Weight: 241.0813

Identification/Properties

Computed Properties
Molecular Weight:
241.084g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
239.979g/mol
Monoisotopic Mass:
239.979g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
217
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(3-Bromophenyl)cyclopropanecarboxylic acid, commonly known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the development of pharmaceuticals, agrochemicals, and fine chemicals due to its unique structure and reactivity.In chemical synthesis, $name$ can undergo various transformations to introduce the 3-bromophenyl and cyclopropane functionalities into new molecules. These transformations include cross-coupling reactions, nucleophilic substitutions, and cycloaddition reactions. The presence of the bromine atom and cyclopropane ring in $name$ also imparts interesting properties to the resulting molecules, making them of interest for further biological and materials studies.One of the key applications of 2-(3-Bromophenyl)cyclopropanecarboxylic acid is in the synthesis of biologically active compounds, where the cyclopropane moiety can serve as a rigid structural element to mimic natural products or optimize drug-like properties. Additionally, the 3-bromophenyl group can act as a handle for further derivatization or functionalization, enabling chemists to fine-tune the properties of the final compounds.Overall, the utilization of 2-(3-Bromophenyl)cyclopropanecarboxylic acid in chemical synthesis offers a powerful tool for designing and synthesizing novel molecules with potential applications in drug discovery, material science, and beyond.