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58553-48-3

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58553-48-3 Usage

General Description

2-Cyano-5-hydroxymethylpyridine is a chemical compound categorized under the class of organic compounds known as pyridines and derivatives. Pyridines are compounds containing a pyridine ring, a six-membered aromatic heterocycle which consists of one nitrogen atom and five carbon atoms. In this specific compound, along with the pyridine ring, it has a cyanide group (carbon triple-bonded to nitrogen) attached at the 2nd position and a hydroxymethyl group (-CH2OH) which is a compound functional group that consists of a hydroxy group (-OH) and methyl group (-CH2-), attached at the 5th position of the pyridine ring. Due to its chemical structure, the properties and applications of the compound can vary widely, potentially used in chemical synthesis or as a building block in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 58553-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,5 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58553-48:
(7*5)+(6*8)+(5*5)+(4*5)+(3*3)+(2*4)+(1*8)=153
153 % 10 = 3
So 58553-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O/c8-3-7-2-1-6(5-10)4-9-7/h1-2,4,10H,5H2

58553-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(hydroxymethyl)pyridine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 5-hydroxymethylpyridine-2-carbonitrile

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:58553-48-3 SDS

58553-48-3Relevant articles and documents

Heterocyclic phosphodiesterase inhibitor and uses thereof

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Paragraph 0159-0163, (2019/11/04)

The present invention belongs to the technical field of medicine, and particularly relates to a heterocyclic phosphodiesterase inhibitor compound represented by a formula (I), or a pharmaceutically acceptable salt and a stereoisomer thereof, and a pharmaceutical preparation, a pharmaceutical composition and applications of the compound, wherein R1, R2, R3, R4, ring A, m and n are defined in the specification. According to the present invention, the compound can be used for preparing drugs for treatment or prevention of diseases associated with PDE9 kinase.

Iminothiadiazine Dioxide Compounds as BACE Inhibitors, Compositions and Their Use

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Paragraph 0589, (2015/11/16)

In its many embodiments, the present invention provides certain iminothiadiazine dioxide compounds, including compounds Formula (I): and include stereoisomers thereof, and pharmaceutically acceptable salts of said compounds stereoisomers, wherein each of R1, R2, R3, R4, R5, R9, ring A, ring B, m, n, p, -L1-, -L2-, and -L3- is selected independently and as defined herein. The novel iminothiadiazine dioxide compounds of the invention have surprisingly been found to exhibit properties which are expected to render them advantageous as BACE inhibitors and/or for the treatment and prevention of various pathologies related to β-amyloid (“Aβ”) production. Pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other active agents), and methods for their preparation and use in treating pathologies associated with amyloid beta (Aβ) protein, including Alzheimer's disease, are also disclosed.

HETEROCYCLIC DERIVATIVES

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Page/Page column 29, (2010/02/13)

The invention relates to novel heterocyclic derivatives, processes for their preparation, and their use in medicaments, especially for the treatment of chronic obstructive pulmonary diseases, acute coronary syndrome, acute myocardial infarction and heart failure development.

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