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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)-2-methylpropanoic acid

Brc1cccc(c1)C(C(=O)O)(C)C Request for Quotation
Chemical Name: 2-(3-bromophenyl)-2-methylpropanoic acid
CAS Number: 81606-47-5
Product Number: AG003ETB(AGN-PC-0NKD1M)
Synonyms:
MDL No: MFCD11036929
Molecular Formula: C10H11BrO2
Molecular Weight: 243.0971

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
243.1g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
241.994g/mol
Monoisotopic Mass:
241.994g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
201
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(3-Bromophenyl)-2-methylpropanoic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique chemical structure enables it to participate in numerous synthetic reactions, making it indispensable in modern organic chemistry.One of the primary applications of 2-(3-Bromophenyl)-2-methylpropanoic acid is as a precursor for the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. By undergoing specific chemical transformations, this compound can be converted into intermediate molecules that are further elaborated to produce these essential medications. Additionally, its involvement in the synthesis of agrochemicals highlights its significance in the development of crop protection agents and agricultural innovations.Furthermore, the versatility of 2-(3-Bromophenyl)-2-methylpropanoic acid extends to the creation of specialty chemicals and advanced materials used in various industries. Its ability to serve as a starting material for the synthesis of complex molecules underscores its importance in the advancement of chemical science and technology.In conclusion, 2-(3-Bromophenyl)-2-methylpropanoic acid plays a pivotal role in chemical synthesis, contributing to the production of pharmaceuticals, agrochemicals, and advanced materials essential for diverse applications. Its versatility and significance as a key building block highlight its critical role in the realm of organic chemistry.