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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)-

4-[5-(4-phenyl-8-propan-2-ylquinolin-2-yl)-1H-pyrrol-2-yl]benzoic acid

OC(=O)c1ccc(cc1)c1ccc([nH]1)c1cc(c2ccccc2)c2c(n1)c(ccc2)C(C)C Request for Quotation
Chemical Name: 4-[5-(4-phenyl-8-propan-2-ylquinolin-2-yl)-1H-pyrrol-2-yl]benzoic acid
CAS Number: 187400-85-7
Product Number: AG00ASXM(AGN-PC-0MYNYH)
Synonyms:
MDL No: MFCD20926333
Molecular Formula: C29H24N2O2
Molecular Weight: 432.5131

Identification/Properties

Computed Properties
Molecular Weight:
432.523g/mol
XLogP3:
6.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
432.184g/mol
Monoisotopic Mass:
432.184g/mol
Topological Polar Surface Area:
66A^2
Heavy Atom Count:
33
Formal Charge:
0
Complexity:
652
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


ER 50891 is a versatile chemical compound that finds wide application in chemical synthesis. This compound is highly valued for its ability to act as a catalyst in various organic reactions, particularly in the field of asymmetric synthesis. One of the key roles of ER 50891 in chemical synthesis is its use as a chiral ligand in transition metal-catalyzed reactions. By serving as a chiral backbone, ER 50891 can effectively control the stereochemistry of the products formed in these reactions, leading to the selective formation of enantiomerically pure compounds. Additionally, ER 50891 can also be employed in other important transformations such as cross-coupling reactions, carbon-carbon bond formations, and functional group interconversions. Its reliable performance and versatility make ER 50891 a valuable tool for chemists working in the field of organic synthesis.