1. Home
  2. 4-Pyridinemethanol, a,a-diphenyl-

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)-

4-Pyridinemethanol, a,a-diphenyl-

OC(c1ccncc1)(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: 4-Pyridinemethanol, a,a-diphenyl-
CAS Number: 1620-30-0
Product Number: AG001SM8(AGN-PC-0Q85XY)
Synonyms:
MDL No:
Molecular Formula: C18H15NO
Molecular Weight: 261.3178

Identification/Properties

Properties
MP:
240 °C
BP:
445.268 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
261.324g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
261.115g/mol
Monoisotopic Mass:
261.115g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
268
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


4-Pyridinemethanol, α,α-diphenyl- is a highly versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. With its aromatic pyridine ring and functional hydroxyl group, this compound serves as a valuable building block in the preparation of various organic molecules.In chemical synthesis, 4-Pyridinemethanol, α,α-diphenyl- can act as a nucleophile or a ligand in transition metal-catalyzed reactions, facilitating the formation of complex structures with high efficiency. Its aromatic nature allows for π-stacking interactions and aromatic substitutions, leading to the synthesis of heterocyclic compounds with diverse functionalities.Furthermore, the presence of the α,α-diphenyl substituents enhances the steric hindrance and electronic properties of the compound, making it a useful reagent in challenging transformations such as asymmetric synthesis and cross-coupling reactions. Overall, 4-Pyridinemethanol, α,α-diphenyl- is a valuable tool in the hands of synthetic chemists for the creation of novel compounds and the exploration of new reaction pathways.