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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)-

(2R)-2-phenyl-2-pyrrol-1-ylacetic acid

OC(=O)C(n1cccc1)c1ccccc1 Request for Quotation
Chemical Name: (2R)-2-phenyl-2-pyrrol-1-ylacetic acid
CAS Number: 105264-23-1
Product Number: AG009T00(AGN-PC-00LRRK)
Synonyms:
MDL No:
Molecular Formula: C12H11NO2
Molecular Weight: 201.2212

Identification/Properties

Computed Properties
Molecular Weight:
201.225g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
201.079g/mol
Monoisotopic Mass:
201.079g/mol
Topological Polar Surface Area:
42.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
218
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-Phenyl-2-(1H-pyrrol-1-yl)acetic acid, also known as $name$ , is a valuable compound in chemical synthesis due to its versatile applications. Its unique structure makes it a useful building block in the creation of various organic molecules. In particular, $name$ serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials with complex molecular architectures. By incorporating $name$ into synthetic routes, chemists can introduce specific functional groups and stereochemistry, leading to the production of novel compounds with tailored properties. Additionally, $name$ can participate in a range of reactions, such as amide formation, Suzuki couplings, and Heck reactions, further expanding its utility in organic synthesis. Overall, the strategic incorporation of $name$ in chemical processes enables the efficient and precise construction of diverse molecular structures, making it a valuable tool for synthetic chemists.