51269-81-9 Usage
General Description
5-Chloropyridine-3-carboxylic acid methyl ester is a chemical compound with the molecular formula C7H6ClNO2. It is a derivative of pyridine and is commonly used in the synthesis of pharmaceuticals and agrochemicals. 5-Chloropyridine-3-carboxylic acid methyl ester is often used as an intermediate in the production of various drugs and is also used as a building block in organic chemistry. It is a colorless liquid with a slightly bitter taste and is soluble in organic solvents. 5-Chloropyridine-3-carboxylic acid methyl ester is considered to be a potentially hazardous chemical and should be handled and disposed of with care.
Check Digit Verification of cas no
The CAS Registry Mumber 51269-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,6 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51269-81:
(7*5)+(6*1)+(5*2)+(4*6)+(3*9)+(2*8)+(1*1)=119
119 % 10 = 9
So 51269-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO2/c1-11-7(10)5-2-6(8)4-9-3-5/h2-4H,1H3
51269-81-9Relevant articles and documents
TRIAZOLE AGONISTS OF THE APJ RECEPTOR
-
Paragraph 0343; 0344, (2016/12/07)
Compounds of Formula I and Formula II, pharmaceutically acceptable salt thereof, stereoisomers of any of the foregoing, or mixtures thereof are agonists of the APJ Receptor and have use in treating cardiovascular and other conditions. Compounds of Formula I and Formula II have the following structures where the definitions of the variables are provided herein.
Benzamides
-
Paragraph 0123, (2014/05/07)
The present invention is directed to benzamide containing compounds which inhibit the P2X7 receptor
SUBSTITUTED (E)-N'-(1-PHENYLETHYLIDENE) BENZOHYDRAZIDE ANALOGS AS HISTONE DEMETHYLASE INHIITORS
-
Page/Page column 93, (2013/03/26)
In one aspect, the invention relates to substituted (E)-N'-(1- phenylethylidene)benzohydrazide analogs, derivatives thereof, and related compounds, which are useful as inhibitors of lysine-specific histone demethylase, including LSD1; synthetic methods fo
