1. Home
  2. 1H-Benzimidazole-5-carboxylicacid, 2-methyl-1-phenyl-

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)-

1H-Benzimidazole-5-carboxylicacid, 2-methyl-1-phenyl-

OC(=O)c1ccc2c(c1)nc(n2c1ccccc1)C Request for Quotation
Chemical Name: 1H-Benzimidazole-5-carboxylicacid, 2-methyl-1-phenyl-
CAS Number: 92437-43-9
Product Number: AG00GS3H(AGN-PC-0JTWXB)
Synonyms:
MDL No:
Molecular Formula: C15H12N2O2
Molecular Weight: 252.2680

Identification/Properties

Computed Properties
Molecular Weight:
252.273g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
252.09g/mol
Monoisotopic Mass:
252.09g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
341
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

Request for Quotation

Customer Feedback

Chemical Structure


2-Methyl-1-phenyl-1H-benzimidazole-5-carboxylic acid, also known as $name$, serves as a versatile building block in chemical synthesis. This compound is commonly employed in the pharmaceutical industry for the creation of novel molecules with potential therapeutic properties. Due to its unique structure and functional groups, $name$ can be utilized as a key intermediate in the synthesis of various biologically active compounds. Its presence in synthesis routes allows for the development of new drug candidates or chemical entities with targeted pharmacological effects. Additionally, $name$ can be functionalized to introduce specific substituents or modify its chemical properties, enabling the generation of diverse molecular analogs for further biological evaluations. This compound plays a vital role in the design and development of potential drug candidates and molecular probes, highlighting its significance in chemical synthesis for pharmaceutical research and development.