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2-Hydroxymethyl-3-methyl-4-nitropyridine, a pyridine derivative with the molecular formula C7H8N2O3, is a chemical compound that features a nitro group and a hydroxymethyl group attached to the pyridine ring. This versatile compound is recognized for its potential applications in various fields, including organic synthesis and pharmaceutical development.

168167-49-5

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168167-49-5 Usage

Uses

Used in Organic Synthesis:
2-Hydroxymethyl-3-methyl-4-nitropyridine is utilized as a key intermediate in organic synthesis, contributing to the creation of a wide range of chemical products. Its unique structure allows for further chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-Hydroxymethyl-3-methyl-4-nitropyridine serves as an intermediate in the production of various drugs. Its presence in the synthesis process is crucial for the development of new medications, potentially leading to advancements in healthcare and treatment options.
Used in Agrochemicals:
2-HYDROXYMETHYL-3-METHYL-4-NITROPYRIDINE also finds application in the agrochemical sector, where it is used as an intermediate in the synthesis of pesticides and other agricultural chemicals. Its role in this industry is vital for enhancing crop protection and ensuring food security.
Used in Fine Chemicals:
2-Hydroxymethyl-3-methyl-4-nitropyridine is employed in the production of fine chemicals, which are high-purity chemicals used in various specialized applications. Its contribution to this field underscores its versatility and importance in the chemical market.
Used in Research and Development:
In the realm of research and development, 2-Hydroxymethyl-3-methyl-4-nitropyridine is a subject of interest for scientists exploring its potential biological activity and applications in medicinal chemistry. Its nitropyridine structure may offer insights into drug discovery and the development of novel therapeutic agents.
As a compound with diverse applications and potential for further exploration, 2-Hydroxymethyl-3-methyl-4-nitropyridine holds promise in contributing to the advancement of various industries, from pharmaceuticals to agrochemicals, and in the ongoing pursuit of scientific knowledge.

Check Digit Verification of cas no

The CAS Registry Mumber 168167-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,1,6 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 168167-49:
(8*1)+(7*6)+(6*8)+(5*1)+(4*6)+(3*7)+(2*4)+(1*9)=165
165 % 10 = 5
So 168167-49-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O3/c1-5-6(4-10)8-3-2-7(5)9(11)12/h2-3,10H,4H2,1H3

168167-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methyl-4-nitropyridin-2-yl)methanol

1.2 Other means of identification

Product number -
Other names 2-Hydroxymethyl-3-methyl-4-nitropyridine

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:168167-49-5 SDS

168167-49-5Downstream Products

168167-49-5Relevant academic research and scientific papers

HETEROCYCLIC COMPOUND

-

, (2015/07/15)

Provided is a compound having a superior FLAP inhibitory action and useful as a prophylactic or therapeutic agent for arteriosclerosis and the like, and a salt thereof. The present invention relates to a compound represented by the formula wherein each symbol is as defined in the present DESCRIPTION, or a salt thereof.

Synthetic studies connected with the preparation of H+/K +-ATPase inhibitors rabeprazole and lansoprazole

Radl, Stanislav,Klecan, Ondrej,Havlicek, Jaroslav

, p. 1447 - 1453 (2007/10/03)

Synthesis of lansoprazole and rabeprazole using common intermediates is devised. The common intermediates, 2-[(4-nitro-3-methylpyridin-2-yl) methanesulfanyl]-1H-benzoimidazole and 2-[(4-chloro-3-methyl-pyridin-2-yl) methanesulfanyl]-1H-benzoimidazole, were prepared in several ways.

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