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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)-

Cyclobutanecarboxylic acid, 1-(4-bromophenyl)-

OC(=O)C1(CCC1)c1ccc(cc1)Br Request for Quotation
Chemical Name: Cyclobutanecarboxylic acid, 1-(4-bromophenyl)-
CAS Number: 151157-49-2
Product Number: AG007F5J(AGN-PC-015QW9)
Synonyms:
MDL No:
Molecular Formula: C11H11BrO2
Molecular Weight: 255.1078

Identification/Properties

Computed Properties
Molecular Weight:
255.111g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
253.994g/mol
Monoisotopic Mass:
253.994g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
227
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#:
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


1-(4-Bromophenyl)cyclobutanecarboxylic acid is a versatile compound commonly used in chemical synthesis due to its unique structure and reactivity. This compound serves as a key building block in organic chemistry, especially in the synthesis of pharmaceuticals, agrochemicals, and materials science.Its cyclobutane ring provides a constrained and rigid structure, making it valuable in the design of biologically active molecules. The presence of the bromophenyl group enhances the compound's potential for cross-coupling reactions, allowing for the introduction of various functional groups with high specificity and efficiency.The carboxylic acid moiety in 1-(4-Bromophenyl)cyclobutanecarboxylic acid is crucial for further derivatization, enabling the modification of the compound through esterification, amidation, or other reactions to tailor its properties for specific applications. Additionally, this carboxylic acid functionality can participate in condensation reactions, leading to the formation of peptide bonds or ester linkages in peptide and drug synthesis.Overall, the strategic positioning of the bromophenyl group and the cyclobutane ring in 1-(4-Bromophenyl)cyclobutanecarboxylic acid makes it a valuable intermediate in organic synthesis, offering opportunities for complexity building and diversification in chemical design.