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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)-

Benzenepropanoic acid, 3,5-dibromo-

OC(=O)CCc1cc(Br)cc(c1)Br Request for Quotation
Chemical Name: Benzenepropanoic acid, 3,5-dibromo-
CAS Number: 923977-15-5
Product Number: AG00H1LC(AGN-PC-00RXC3)
Synonyms:
MDL No:
Molecular Formula: C9H8Br2O2
Molecular Weight: 307.9666

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(3,5-Dibromophenyl)propanoic acid serves as a versatile building block in chemical synthesis, particularly in the field of organic chemistry. This compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique chemical structure and reactivity. By incorporating 3-(3,5-Dibromophenyl)propanoic acid into synthetic routes, chemists can introduce specific functionalities and structural motifs into target molecules, thereby influencing their properties and behavior. Additionally, this compound can participate in a range of transformations such as Suzuki coupling, Heck reaction, and Grignard reactions, expanding its utility in the synthesis of complex organic compounds.