1. Home
  2. 2-methyl-2-[4-(trifluoromethyl)phenyl]propanoic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-methyl-2-[4-(trifluoromethyl)phenyl]propanoic acid

OC(=O)C(c1ccc(cc1)C(F)(F)F)(C)C Request for Quotation
Chemical Name: 2-methyl-2-[4-(trifluoromethyl)phenyl]propanoic acid
CAS Number: 32445-89-9
Product Number: AG00BZIV(AGN-PC-03EUTS)
Synonyms:
MDL No:
Molecular Formula: C11H11F3O2
Molecular Weight: 232.1990

Identification/Properties

Computed Properties
Molecular Weight:
232.202g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
232.071g/mol
Monoisotopic Mass:
232.071g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
263
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Methyl-2-(4-(trifluoromethyl)phenyl)propanoic acid, also known as $name$, is a versatile compound frequently used in chemical synthesis. Its distinctive structure enables it to serve as a key building block in the creation of various organic molecules.One prevalent application of 2-Methyl-2-(4-(trifluoromethyl)phenyl)propanoic acid in chemical synthesis is its role as a precursor in the production of pharmaceuticals. By incorporating this compound into the synthesis process, chemists can introduce specific functional groups and stereochemistry into drug molecules, influencing their biological activity and pharmacological properties.Additionally, 2-Methyl-2-(4-(trifluoromethyl)phenyl)propanoic acid can act as a synthetic intermediate in the preparation of agrochemicals, polymers, and specialty chemicals. Its unique reactivity and structural features make it an invaluable tool for designing and synthesizing complex organic compounds with tailored properties for various applications.Overall, the strategic use of 2-Methyl-2-(4-(trifluoromethyl)phenyl)propanoic acid in chemical synthesis plays a crucial role in advancing diverse fields such as pharmaceuticals, agrochemicals, and materials science.