76915-53-2 Usage
General Description
(2-Methyl-pyridin-3-yl)-methanol, also known as 2-Methyl-3-pyridylmethanol, is a chemical compound with the molecular formula C8H9NO. It is a colorless liquid with a molecular weight of 135.16 g/mol. (2-METHYL-PYRIDIN-3-YL)-METHANOL is commonly used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It contains a pyridine ring and a hydroxyl group, making it a versatile building block for the synthesis of various organic compounds. Additionally, it has been found to exhibit some biological activity and is being researched for its potential applications in medicine and agriculture. However, it is important to handle this compound with care, as it may pose health and environmental risks if not properly managed.
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.
76915-53-2Relevant articles and documents
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.
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
