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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-Pyridinecarboxamide, 1,4-dihydro-1-(phenylmethyl)-

NC(=O)C1=CN(C=CC1)Cc1ccccc1 Request for Quotation
Chemical Name: 3-Pyridinecarboxamide, 1,4-dihydro-1-(phenylmethyl)-
CAS Number: 952-92-1
Product Number: AG003DZA(AGN-PC-0JM179)
Synonyms:
MDL No:
Molecular Formula: C13H14N2O
Molecular Weight: 214.2631

Identification/Properties

Properties
MP:
121°C
BP:
433.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
214.268g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
214.111g/mol
Monoisotopic Mass:
214.111g/mol
Topological Polar Surface Area:
46.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
314
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Benzyl-1,4-dihydronicotinamide, also known as BNAH, is a versatile chemical compound commonly used in chemical synthesis for a variety of applications. As a reducing agent, BNAH is particularly valued for its ability to efficiently and selectively reduce a wide range of functional groups, such as ketones, aldehydes, and imines. This makes it a key reagent in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, BNAH is known for its stability, ease of use, and environmentally friendly profile, making it a preferred choice for many synthetic chemists. With its broad utility and effectiveness in various reactions, 1-Benzyl-1,4-dihydronicotinamide plays a crucial role in modern chemical synthesis.