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6456-44-6

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6456-44-6 Usage

Description

1-METHYL-NICOTINAMIDE IODIDE is a nicotinic acid derivative that exhibits dopaminergic neurotoxicity.

Uses

Used in Pharmaceutical Research:
1-METHYL-NICOTINAMIDE IODIDE is used as a research compound for studying its dopaminergic neurotoxic effects and potential applications in the development of treatments for neurological disorders.
Used in Chemical Synthesis:
1-METHYL-NICOTINAMIDE IODIDE is used as a chemical intermediate in the synthesis of other nicotinic acid derivatives and related compounds for various applications in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6456-44-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6456-44:
(6*6)+(5*4)+(4*5)+(3*6)+(2*4)+(1*4)=106
106 % 10 = 6
So 6456-44-6 is a valid CAS Registry Number.
InChI:InChI=1/C26H26N2O5/c1-31-22-10-5-11-23(32-2)24(22)26(30)28-27-25(29)20-9-3-6-17(14-20)16-33-21-13-12-18-7-4-8-19(18)15-21/h3,5-6,9-15H,4,7-8,16H2,1-2H3,(H,27,29)(H,28,30)

6456-44-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyl-nicotinamide Iodide

1.2 Other means of identification

Product number -
Other names 1-METHYL-NICOTINAMIDE IODIDE

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:6456-44-6 SDS

6456-44-6Relevant articles and documents

Metal-free reduction of unsaturated carbonyls, quinones, and pyridinium salts with tetrahydroxydiboron/water

Li, Tiejun,Peng, Henian,Tang, Wenjun,Tian, Duanshuai,Xu, Guangqing,Yang, He

, p. 4327 - 4337 (2021/05/31)

A series of unsaturated carbonyls, quinones, and pyridinium salts have been effectively reduced to the corresponding saturated carbonyls, dihydroxybenzenes, and hydropyridines in moderate to high yields with tetrahydroxydiboron/water as a mild, convenient, and metal-free reduction system. Deuterium-labeling experiments have revealed this protocol to be an exclusive transfer hydrogenation process from water. This journal is

An improved method for the quaternization of nicotinamide and antifungal activities of its derivatives

Siber, Tamara,Bu?i?, Valentina,Zobund?ija, Dora,Roca, Sun?ica,Viki?-Topi?, Dra?en,Vrande?i?, Karolina,Ga?o-Soka?, Dajana

, (2019/03/26)

The quaternization reactions of nicotinamide, with different electrophiles: methyl iodide and substituted 2-bromoacetophenones (4-Cl, 4-Br, 4-H, 4-CH3, 4-F, 4-OCH3, 4-Ph, 2-OCH3, 4-NO2) are reported. The preparations were carried out by conventional synthesis and under microwave irradiation in absolute ethanol and acetone. The synthesis performed by microwave dielectric heating significantly improved yield, up to 8 times, and shortened down the reaction time from ca. one day in conventional, to 10–20 min. The structures of the synthesized compounds were confirmed by IR, 1H- and 13C-NMR spectroscopy, mass spectrometry and elemental analysis. The compounds have been screened for antifungal activities against Fusarium oxysporum, Fusarium culmorum, Macrophomina phaseolina and Sclerotinia sclerotiorum at concentrations of 10 μg/mL and 100 μg/mL. Six compounds showed the strong inhibition of mycelium growth at a concentration of 10 μg/mL. All tested compounds revealed the great inhibitory activities against S. sclerotiorum at a concentration of 100 μg/mL.

A combined experimental and theoretical study of the pH-dependent binding mode of NAD+ by water-soluble molecular clips

Polkowska, Jolanta,Bastkowski, Frank,Schrader, Thomas,Klaerner, Frank-Gerrit,Zienau, Jan,Koziol, Felix,Ochsenfeld, Christian

supporting information; scheme or table, p. 779 - 790 (2010/06/13)

The highly selective recognition process of NAD+ and NADH (as important cofactors of many redox enzymes) by molecular clips in aqueous solution is studied systematically by a combined experimental and quantum-chemical approach. The strongly pH-

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