Welcome to LookChem.com Sign In|Join Free
  • or
N-BENZYLNICOTINAMIDE is a chemical compound that belongs to the nicotinamide family, a derivative of nicotinamide, which is a form of vitamin B3. It is known for its antioxidant and neuroprotective properties and is commonly used in research and studies related to the treatment of neurological disorders, metabolic diseases, and cancer. N-BENZYLNICOTINAMIDE is also being investigated for its ability to improve mitochondrial function and energy metabolism, making it a promising candidate for therapeutic interventions targeting these pathways. Overall, N-benzylnicotinamide shows potential as a valuable compound for medicinal and pharmaceutical purposes.

2503-55-1

Post Buying Request

2503-55-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2503-55-1 Usage

Uses

Used in Pharmaceutical Industry:
N-BENZYLNICOTINAMIDE is used as a research compound for the development of new drugs for various medical conditions, particularly in the treatment of neurological disorders, metabolic diseases, and cancer.
Used in Neurological Disorders Research:
N-BENZYLNICOTINAMIDE is used as a neuroprotective agent in studies related to the treatment of neurological disorders, due to its antioxidant and neuroprotective properties.
Used in Metabolic Diseases Research:
N-BENZYLNICOTINAMIDE is used as a research compound in studies related to the treatment of metabolic diseases, given its potential to improve mitochondrial function and energy metabolism.
Used in Cancer Research:
N-BENZYLNICOTINAMIDE is used as a research compound in studies related to the treatment of cancer, as it has been shown to possess potential applications in this area.

Check Digit Verification of cas no

The CAS Registry Mumber 2503-55-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,0 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2503-55:
(6*2)+(5*5)+(4*0)+(3*3)+(2*5)+(1*5)=61
61 % 10 = 1
So 2503-55-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO/c10-7-9-6-8-4-2-1-3-5-8/h1-5,7H,6H2,(H,9,10)

2503-55-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-BENZYLNICOTINAMIDE

1.2 Other means of identification

Product number -
Other names nicotinic acid benzylamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2503-55-1 SDS

2503-55-1Relevant academic research and scientific papers

Reductive N-alkylation of primary amides using nickel-nanoparticles

Alenad, Asma M.,Alshammari, Ahmad S.,Jagadeesh, Rajenahally V.,Murugesan, Kathiravan,Sohail, Manzar

, (2021/11/22)

Here we report Ni-nanoparticles as reusable catalysts for reductive N-alkylation of amides. These Ni-nanoparticles based catalysts have been prepared by the template synthesis of tartaric acid and 2-methyl imidazole ligated Ni-complex on SiO2 and subsequent pyrolysis under argon. Applying optimal Ni-nanostructured catalyst, N-alkylation of aromatic and heterocyclic primary amides with different aldehydes in presence of molecular hydrogen was performed to access structurally diverse N-alkylated amides in good to excellent yields. In addition, the applicability of this N-alkylation protocol has been demonstrated for the selective functionalization of primary amide group in Levetiracetam drug.

Water-promoted dehydrative coupling of 2-aminopyridines in heptane: Via a borrowing hydrogen strategy

Azumaya, Isao,Hikawa, Hidemasa,Kikkawa, Shoko,Nakayama, Taku

, p. 23144 - 23150 (2021/07/21)

A synthetic method for dehydrative N-benzylation promoted by water molecules in heptane using a π-benzylpalladium system has been developed. The presence of water significantly accelerates carbon-nitrogen bond formation, which is accomplished in an atom-economical process to afford the corresponding N-monobenzylated products. A crossover experiment afforded H/D scrambled products, which is consistent with a borrowing hydrogen mechanism. Kinetic isotope effect measurements revealed that benzylic carbon-hydrogen bond cleavage was the rate-determining step.

Ammonia-borane as a Catalyst for the Direct Amidation of Carboxylic Acids

Ramachandran, P. Veeraraghavan,Hamann, Henry J.

supporting information, p. 2938 - 2942 (2021/05/04)

Ammonia-borane serves as an efficient substoichiometric (10%) precatalyst for the direct amidation of both aromatic and aliphatic carboxylic acids. In situ generation of amine-boranes precedes the amidation and, unlike the amidation with stoichiometric amine-boranes, this process is facile with 1 equiv of the acid. This methodology has high functional group tolerance and chromatography-free purification but is not amenable for esterification. The latter feature has been exploited to prepare hydroxyl- and thiol-containing amides.

Graphene oxide: A convenient metal-free carbocatalyst for facilitating amidation of esters with amines

Patel, Khushbu P.,Gayakwad, Eknath M.,Shankarling, Ganapati S.

, p. 2661 - 2668 (2020/02/20)

Herein, we report a graphene oxide (GO) catalyzed condensation of non-activated esters and amines, that can enable diverse amides to be synthesized from abundant ethyl esters forming only volatile alcohol as a by-product. GO accelerates ester to amide conversion in the absence of any additives, unlike other catalysts. A wide range of ester and amine substrates are screened to yield the respective amides in good to excellent yields. The improved catalytic activity can be ascribed to the oxygenated functionalities present on the graphene oxide surface which forms H-bonding with the reactants accelerating the reaction. Improved yields and a wide range of functional group tolerance are some of the important features of the developed protocol.

Nickel-catalyzed reductive amidation of aryl-triazine ethers

Heravi, Majid M.,Panahi, Farhad,Iranpoor, Nasser

supporting information, p. 1992 - 1995 (2020/02/22)

The reaction of activated phenolic compounds, 2,4,6-triaryloxy-1,3,5-triazine (aryl-triazine ethers), with various isocyanates or carbodiimides in the presence of a nickel pre-catalyst resulted in the synthesis of aryl amides in good to excellent yields.

Solvent-Free N-Alkylation of Amides with Alcohols Catalyzed by Nickel on Silica–Alumina

Charvieux, Aubin,Le Moigne, Louis,Borrego, Lorenzo G.,Duguet, Nicolas,Métay, Estelle

supporting information, p. 6842 - 6846 (2019/11/11)

The N-alkylation of phenylacetamide with benzyl alcohol has been studied using Ni/SiO2–Al2O3. In the optimized conditions, the desired product was isolated in an excellent 98 % yield. The reaction could advantageously be performed in neat conditions, with a slight excess of amide and a catalytic amount of base. These conditions were tested on a large range of amides and alcohols, affording 24 compounds in 13 to 99 % isolated yields.

Water-Tolerant and Atom Economical Amide Bond Formation by Metal-Substituted Polyoxometalate Catalysts

De Azambuja, Francisco,Parac-Vogt, Tatjana N.

, p. 10245 - 10252 (2019/11/03)

A simple, safe, and inexpensive amide bond formation directly from nonactivated carboxylic acids and free amines is presented in this work. Readily available Zr(IV)- and Hf(IV)-substituted polyoxometalates (POM) are shown to be catalysts for the amide bond formation reaction under mild conditions, low catalyst loading, and without the use of water scavengers, dry solvents, additives for facilitating the amine attack, or specialized experimental setups commonly employed to remove water. Detailed mechanistic investigations revealed the key role of POM scaffolds which act as inorganic ligands to protect Zr(IV) and Hf(IV) Lewis acidic metals against hydrolysis and preserve their catalytic activity in amide bond formation reactions. The catalysts are compatible with a range of functional groups and heterocycles useful for medicinal, agrochemical, and material chemists. The robustness of the Lewis acid-POM complexes is further supported by the catalyst reuse without loss of activity. This prolific combination of Zr(IV)/Hf(IV) and POMs inaugurates a powerful class of catalysts for the amide bond formation, which overcomes key limitations of previously established Zr(IV)/Hf(IV) salts and boron-based catalysts.

All Non-Carbon B3NO2 Exotic Heterocycles: Synthesis, Dynamics, and Catalysis

Opie, Christopher R.,Noda, Hidetoshi,Shibasaki, Masakatsu,Kumagai, Naoya

supporting information, p. 4648 - 4653 (2019/03/17)

The B3NO2 six-membered heterocycle (1,3-dioxa-5-aza-2,4,6-triborinane=DATB), comprising three different non-carbon period 2 elements, has been recently demonstrated to be a powerful catalyst for dehydrative condensation of carboxylic acids and amines. The tedious synthesis of DATB, however, has significantly diminished its utility as a catalyst, and thus the inherent chemical properties of the ring system have remained virtually unexplored. Here, a general and facile synthetic strategy that harnesses a pyrimidine-containing scaffold for the reliable installation of boron atoms is disclosed, giving rise to a series of Pym-DATBs from inexpensive materials in a modular fashion. The identification of a soluble Pym-DATB derivative allowed for the investigation of the dynamic nature of the B3NO2 ring system, revealing differential ring-closing and -opening behaviors depending on the medium. Readily accessible Pym-DATBs proved their utility as efficient catalysts for dehydrative amidation with broad substrate scope and functional-group tolerance, offering a general and practical catalytic alternative to reagent-driven amidation.

Synthesis, biological evaluation and in silico studies of tetrazole-heterocycle hybrids

Sribalan, Rajendran,Banuppriya, Govindharasu,Kirubavathi, Maruthan,Padmini, Vediappen

, p. 577 - 586 (2018/09/14)

The series of three different chemical entities of tetrazole-heterocycle hybrids such as thiophene, pyridine and quinoline tetrazoles were synthesized and characterized for the purpose to develop new lead molecules. Biological evaluations such as in vitro antimicrobial and anti-inflammatory activities were studied. Further, the in silico studies such as Molecular docking (with COX-1, COX-2 and 3TTZ), DFT calculations, the Molecular electrostatic potential (MEP) and ADME were investigated.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2503-55-1