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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)-

3,3,3-Triphenylpropionic acid

OC(=O)CC(c1ccccc1)(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: 3,3,3-Triphenylpropionic acid
CAS Number: 900-91-4
Product Number: AG003IBU(AGN-PC-0WALIA)
Synonyms:
MDL No:
Molecular Formula: C21H18O2
Molecular Weight: 302.3664

Identification/Properties

Properties
MP:
179-183 °C
BP:
433.6°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
302.373g/mol
XLogP3:
4.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
302.131g/mol
Monoisotopic Mass:
302.131g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
326
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


3,3,3-Triphenylpropanoic acid is a versatile compound widely used in chemical synthesis. It serves as a key building block in the production of various pharmaceuticals, agrochemicals, and advanced materials. In organic synthesis, 3,3,3-Triphenylpropanoic acid is commonly employed as a starting material for the preparation of intricate molecules due to its unique structure and reactivity. Its functional groups allow for diverse chemical transformations, such as esterification, amidation, and oxidation, enabling the creation of complex organic frameworks. Additionally, this compound can be utilized as a chiral auxiliary in asymmetric synthesis to control the stereochemistry of a reaction and selectively produce enantiopure compounds. Overall, the application of 3,3,3-Triphenylpropanoic acid in chemical synthesis highlights its significance in enabling the efficient construction of valuable compounds with tailored properties.