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CAS

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15828-08-7

N-tert-Butylnicotinamide, also known as tBNA, is a chemical compound belonging to the class of nicotinamide derivatives. It is a derivative of nicotinamide, a form of vitamin B3, and is recognized for its versatile applications in both industrial and potential medicinal fields.

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  • 15828-08-7 Structure

  • Basic information

    1. Product Name: N-tert-Butylnicotinamide
    2. Synonyms: N-tert-Butylnicotinamide
    3. CAS NO:15828-08-7
    4. Molecular Formula: C10H14N2O
    5. Molecular Weight: 178.23096
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15828-08-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Inert atmosphere,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: N-tert-Butylnicotinamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-tert-Butylnicotinamide(15828-08-7)
    11. EPA Substance Registry System: N-tert-Butylnicotinamide(15828-08-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 15828-08-7(Hazardous Substances Data)

15828-08-7 Usage

Uses

Used in Corrosion Inhibition:
N-tert-Butylnicotinamide is used as a corrosion inhibitor for protecting metal surfaces from degradation. It is particularly effective in industries such as automotive and aerospace, where metal surfaces require robust protection against environmental factors that can cause corrosion.
Used in Lubricant and Metalworking Fluid Formulation:
In the lubricant and metalworking fluid industries, N-tert-Butylnicotinamide is used as an additive to enhance the anti-corrosive properties of these products. This helps in extending the life of machinery and equipment by reducing wear and tear caused by friction and corrosion.
Used in Pharmaceutical Research:
N-tert-Butylnicotinamide is also being studied for its potential pharmaceutical applications, including its anti-inflammatory and antioxidant properties. These properties make it a promising candidate for the development of new drugs to treat various inflammatory and oxidative stress-related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 15828-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,2 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15828-08:
(7*1)+(6*5)+(5*8)+(4*2)+(3*8)+(2*0)+(1*8)=117
117 % 10 = 7
So 15828-08-7 is a valid CAS Registry Number.

15828-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-Butylnicotinamide

1.2 Other means of identification

Product number -
Other names N-tert-butylpyridine-3-carboxamide

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:15828-08-7 SDS

15828-08-7Downstream Products

15828-08-7Relevant articles and documents

Homogeneous catalytic aminocarbonylation of nitrogen-containing iodo-heteroaromatics. Synthesis of N-substituted nicotinamide related compounds

Takács, Attila,Jakab, Balázs,Petz, Andrea,Kollár, László

, p. 10372 - 10378 (2008/02/13)

Various primary and secondary amines, including amino acid methyl esters, were used as nucleophiles in palladium-catalysed aminocarbonylation of 2-iodopyridine, 3-iodopyridine and iodopyrazine. N-Substituted nicotinamides and 3-pyridyl-glyoxylamides (2-oxo-carboxamide type derivatives) of potential biological importance can be obtained from 3-iodopyridine as a result of simple and double carbon monoxide insertions, respectively. The latter examples can be obtained in synthetically acceptable yields by using elevated carbon monoxide pressure. On the contrary, N-alkyl/aryl-carboxamides were obtained exclusively in the whole pressure range by using 2-iodopyridine and iodopyrazine.

An efficient method for the conversion of aromatic and aliphatic nitriles to the corresponding N-tert-butyl amides: A modified Ritter reaction

Reddy, K. Laxma

, p. 1453 - 1455 (2007/10/03)

Aromatic and aliphatic nitriles react with tert-butyl acetate in the presence of a catalytic amount of sulfuric acid to give the corresponding N-tert-butyl amides in excellent yields.

Improved synthesis of N-substituted 2,3-pyridine-dicarboximides with microwave irradiation

Blanco, Maria M.,Levin, Gustavo J.,Schapira, Celia B.,Perillo, Isabel A.

, p. 1881 - 1890 (2007/10/03)

The microwave-induced synthesis of N-substituted 2,3- pyridinedicarboximides (1) by means of two different approaches is presented. One involves direct N-alkylation of quinolinimide (2) (Method A) and the other, dehydrative condensation of quinolinic anhydride (4) and amines (Method B). Reactions resulted highly accelerated, with improved yields in relation to those obtained by conventional heating. The scope and limitations of each method and its variants are discussed.

Amide derivative

-

, (2008/06/13)

A compound of the formula: wherein Ar is optionally substituted phenyl, etc.; n is 0, 1 or 2; R1is hydogen atom, optionally substituted alkyl, etc.; R2and R3are independently optionally substituted alkyl, etc.; R4and R5are independently hydrogen atom or optionally substituted alkyl; R6is hydrogen atom, hydroxy or alkyl; or a pharmaceutically acceptable salt thereof is useful as a medicament for treating retinal degenerative disorders and the like.

Reaction of magnesiated bases on substituted pyridines: Deprotonation or 1,4-addition?

Bonnet, Veronique,Mongin, Florence,Trecourt, Francois,Queguiner, Guy

, p. 4245 - 4249 (2007/10/03)

N-(tert-Butyl)pyridine-2-carboxamide (1), N-phenylpyridine-2-carboxamide (7) and 2,2-dimethyl-N-(2-pyridyl)-propanamide (18) are readily deprotonated at C3 with a stoichiometric amount of PriMgCl or Bu2Mg in THF under reflux. Subsequ

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