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(2-METHYL-PYRIDIN-3-YL)-METHANOL, also known as 2-Methyl-3-pyridylmethanol, is a colorless liquid chemical compound with the molecular formula C8H9NO and a molecular weight of 135.16 g/mol. It features a pyridine ring and a hydroxyl group, making it a versatile intermediate in organic synthesis for the production of pharmaceuticals and agrochemicals. Its unique structure endows it with potential biological activity, which is currently under investigation for applications in medicine and agriculture. However, due to its potential health and environmental risks, careful handling is required.

76915-53-2

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76915-53-2 Usage

Uses

Used in Pharmaceutical Industry:
(2-METHYL-PYRIDIN-3-YL)-METHANOL is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its ability to serve as a versatile building block in organic synthesis. Its presence in the molecular structure of target drugs can contribute to their therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, (2-METHYL-PYRIDIN-3-YL)-METHANOL is utilized as an intermediate for the development of agrochemicals, potentially enhancing the efficacy of pesticides or other agricultural products by incorporating its unique structural features.
Used in Research and Development:
(2-METHYL-PYRIDIN-3-YL)-METHANOL is employed as a subject of research for its potential biological activity, with ongoing investigations into its applications in medicine and agriculture to explore its full potential and possible benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 76915-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,1 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76915-53:
(7*7)+(6*6)+(5*9)+(4*1)+(3*5)+(2*5)+(1*3)=162
162 % 10 = 2
So 76915-53-2 is a valid CAS Registry Number.

76915-53-2SDS

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-(bromomethyl)-2-methylpyridine

1.2 Other means of identification

Product number -
Other names -

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:76915-53-2 SDS

76915-53-2Relevant academic research and scientific papers

Novel heterocyclic derivative capable of being used as SHP2 inhibitor

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Paragraph 0310, (2019/08/30)

The invention relates to a novel heterocyclic derivative capable of being used as an SHP2 inhibitor, specifically relates to a compound shown by a formula I or pharmaceutically acceptable salts thereof, further relates to a use of the compound shown by the formula I or the pharmaceutically acceptable salts thereof and a pharmaceutical composition thereof in drug preparation, and particularly relates to a use in preparation of drugs for treatment, inhibition or prevention of diseases or discomforts mediated by SHP2 activity.

NOVEL HETEROCYCLIC DERIVATIVES USEFUL AS SHP2 INHIBITORS

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Page/Page column 66, (2018/10/19)

This invention relates to certain novel pyrazine derivatives (Formula I) as SHP2 inhibitors which is shown as formula I, their synthesis and their use for treating a SHP2 mediated disorder. More particularly, this invention is directed to fused heterocyclic group derivatives useful as inhibitors of SHP2, methods for producing such compounds and methods for treating a SHP2-mediated disorder.

Regioselectivity in free radical bromination of unsymmetrical dimethylated pyridines

Thapa, Rajesh,Brown, Jordan,Balestri, Thomas,Taylor, Richard T.

supporting information, p. 6743 - 6746 (2015/01/09)

During a literature review some curious inconsistencies in the free radical bromination of picolines were noted. To achieve a better understanding of the mechanisms and regioselectivity we reran these reactions, extending our work to unsymmetrical lutidin

Synthesis of Functionalized Quinoline Derivatives by Annulation of Pyridines

Ghera, Eugene,David, Yoshua Ben,Rapoport, Henry

, p. 2059 - 2065 (2007/10/02)

Thiophenyl and sulfonylphenyl groups were introduced on each methyl group of 2,3-lutidine (1), and the reactivity of the adjacent carbanions has been examined.When both methyl groups of 1 were substituted with sulfur groups, regioselective alkylation of t

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