952-92-1 | 1-Benzyl-1,4-dihydronicotinamide

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$29.00	$21.00
5g	98%	in stock	$69.00	$49.00
10g	98%	in stock	$138.00	$97.00
15g	98%	in stock	$203.00	$143.00
25g	98%	in stock	$334.00	$234.00

Description

• Catalog Number: AB57886
• Chemical Name: 1-Benzyl-1,4-dihydronicotinamide
• CAS Number: 952-92-1
• Molecular Formula: C13H14N2O
• Molecular Weight: 214.2631
• MDL Number: MFCD00059769
• SMILES: NC(=O)C1=CN(C=CC1)Cc1ccccc1
• NSC Number: 26899

Computed Properties

• Complexity: 314
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 1.4

Literature

• Magnetic nano-Fe3O4-supported 1-benzyl-1,4-dihydronicotinamide (BNAH): synthesis and application in the catalytic reduction of α,β-epoxy ketones.

  Organic letters 20120302

• Cupric superoxo-mediated intermolecular C-H activation chemistry.

  Journal of the American Chemical Society 20110216

• Old and new inhibitors of quinone reductase 2.

  Chemico-biological interactions 20100730

• Sequential electron-transfer and proton-transfer pathways in hydride-transfer reactions from dihydronicotinamide adenine dinucleotide analogues to non-heme oxoiron(IV) complexes and p-chloranil. Detection of radical cations of NADH analogues in acid-promoted hydride-transfer reactions.

  Journal of the American Chemical Society 20081112

• Electron-transfer and acid-base properties of a two-electron oxidized form of quaterpyrrole that acts as both an electron donor and an acceptor.

  The journal of physical chemistry. A 20080221

• Supramolecular carbon nanotube-fullerene donor-acceptor hybrids for photoinduced electron transfer.

  Journal of the American Chemical Society 20071226

• Nanostructural control of cup-stacked carbon nanotubes with 1-benzyl-1,4-dihydronicotinamide dimer via photoinduced electron transfer.

  Chemical communications (Cambridge, England) 20070107

• Self-assembled single-walled carbon nanotube:zinc-porphyrin hybrids through ammonium ion-crown ether interaction: construction and electron transfer.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

• Mechanistic borderline between one-step hydrogen transfer and sequential transfers of electron and proton in reactions of NADH analogues with triplet excited states of tetrazines and Ru(bpy)(3)2+.

  Journal of the American Chemical Society 20061108

• Negative kinetic temperature effect on the hydride transfer from NADH analogue BNAH to the radical cation of N-benzylphenothiazine in acetonitrile.

  The Journal of organic chemistry 20060901

• Catalytic hydrogenation of alpha,beta-epoxy ketones to form beta-hydroxy ketones mediated by an NADH coenzyme model.

  Organic letters 20060803

• Efficient photoreduction process of [Ru3(mu3-O)(mu-CH3CO2)6L3]+ by electron-mediation via the viologen dication by excitation of a zinc porphyrin.

  Inorganic chemistry 20051114

• Hydroxyl radical generation via photoreduction of a simple pyridine N-oxide by an NADH analogue.

  Organic & biomolecular chemistry 20050921

• Transition metal complexes coordinated by an NAD(P)H model compound and their enhanced hydride-donating abilities in the presence of a base.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20050704

• Architecture of supramolecular metal complexes for photocatalytic CO2 reduction: ruthenium-rhenium bi- and tetranuclear complexes.

  Inorganic chemistry 20050404

• Hydricities of BzNADH, CH5Mo(PMe3)(CO)2H, and C5Me5Mo(PMe3)(CO)2H in acetonitrile.

  Journal of the American Chemical Society 20040310

• Reversed effects of DNA on hydride transfer and electron transfer reactions of acridinium and quinolinium ions.

  Chemical communications (Cambridge, England) 20030807

• Mechanisms of electron-transfer oxidation of NADH analogues and chemiluminescence. Detection of the keto and enol radical cations.

  Journal of the American Chemical Society 20030423

• Polysiloxane-supported NAD(P)H model 1-benzyl-1,4-dihydronicotinamide: synthesis and application in the reduction of activated olefins.

  The Journal of organic chemistry 20030418

• Determination of the C4-H bond dissociation energies of NADH models and their radical cations in acetonitrile.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20030217

• Direct detection of radical cations of NADH analogues.

  Journal of the American Chemical Society 20021211

• Bioorganometallic chemistry. 13. Regioselective reduction of NAD(+) models, 1-benzylnicotinamde triflate and beta-nicotinamide ribose-5'-methyl phosphate, with in situ generated [CpRh(Bpy)H](+): structure-activity relationships, kinetics, and mechanistic aspects in the formation of the 1,4-NADH derivatives.

  Inorganic chemistry 20011217

• Metal ion-catalyzed cycloaddition vs hydride transfer reactions of NADH analogues with p-benzoquinones.

  Journal of the American Chemical Society 20011024

• Photochemical generation of cyclopentadienyliron dicarbonyl anion by a nicotinamide adenine dinucleotide dimer analogue.

  Inorganic chemistry 20010312

• Stereoselective reduction with NADH model BNAH through chiral induction in cyclodextrins.

  Bioorganic chemistry 20010201