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4-Chloro-6-Methylnicotinic acid, also known as 4-Chloro-6-methylpyridine-3-carboxylic acid, is an organic compound and a derivative of nicotinic acid, which is a B vitamin (vitamin B3) that supports human health. This synthetic chemical compound is characterized by its light yellow crystalline solid appearance, a molecular weight of 172.57 g/mol, and a density of 1.43g/cm3. It is not naturally produced but is synthesized in laboratories and is commonly used in the fields of medicine and pharmaceuticals as a key ingredient in the manufacture of more complex organic compounds.

1060805-95-9

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1060805-95-9 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-6-Methylnicotinic acid is used as a key ingredient in the pharmaceutical industry for the synthesis of more complex organic compounds. Its unique chemical structure and properties make it a valuable component in the development of new drugs and medications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 4-Chloro-6-Methylnicotinic acid is utilized as a building block for the design and synthesis of novel therapeutic agents. Its versatile chemical properties allow for the creation of new molecules with potential applications in treating various diseases and medical conditions.
Used in Drug Development:
4-Chloro-6-Methylnicotinic acid plays a crucial role in drug development, where it serves as a precursor or intermediate in the synthesis of pharmaceutical compounds. Its presence in the molecular structure can impart specific biological activities, making it an essential component in the development of new drugs with improved efficacy and safety profiles.
Used in Chemical Synthesis:
As a synthetic chemical compound, 4-Chloro-6-Methylnicotinic acid is also used in various chemical synthesis processes. Its reactivity and functional groups make it a suitable candidate for the preparation of a wide range of chemical products, including dyes, pigments, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1060805-95-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,0,8,0 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1060805-95:
(9*1)+(8*0)+(7*6)+(6*0)+(5*8)+(4*0)+(3*5)+(2*9)+(1*5)=129
129 % 10 = 9
So 1060805-95-9 is a valid CAS Registry Number.

1060805-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-6-methylnicotinic acid

1.2 Other means of identification

Product number -
Other names 4-chloro-6-methylpyridine-3-carboxylic acid

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:1060805-95-9 SDS

1060805-95-9Relevant academic research and scientific papers

Observation of the selective staining of chromosomal DNA in dividing cells using a luminescent terbium(iii) complex

Law, Ga-Lai,Man, Cornelia,Parker, David,Walton, James W.

supporting information; experimental part, p. 2391 - 2393 (2010/08/05)

The emission intensity of a monocationic Tb or Eu(iii) complex of a bis(1-azaxanthone) ligand is enhanced in the presence of serum albumin; the lanthanide complex stains dividing cells, allowing visualisation of mitotic chromosomes. The Royal Society of Chemistry.

PROLYL HYDROXYLASE INHIBITORS

-

Page/Page column 13-14, (2010/07/10)

The invention described herein relates to certain 2,4-dioxo-1,2,3,4-tetrahydropyrido[4,3-d]pyrimidme-7-carboxamide derivatives of formula (I) which are antagonists of HIF prolyl hydroxylases and are useful for treating diseases benefiting from the inhibition of this enzyme, anemia being one example.

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