Cas 1269662-35-2,methyl 4-amino-6-methyl-1-p-tolyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

1269662-35-2

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Basic information

Product Name: methyl 4-amino-6-methyl-1-p-tolyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate
Synonyms: methyl 4-amino-6-methyl-1-p-tolyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate
CAS NO:1269662-35-2
Molecular Formula:
Molecular Weight: 296.329
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: methyl 4-amino-6-methyl-1-p-tolyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 4-amino-6-methyl-1-p-tolyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(1269662-35-2)
EPA Substance Registry System: methyl 4-amino-6-methyl-1-p-tolyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate(1269662-35-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1269662-35-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1269662-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,6,6 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1269662-35:
(9*1)+(8*2)+(7*6)+(6*9)+(5*6)+(4*6)+(3*2)+(2*3)+(1*5)=192
192 % 10 = 2
So 1269662-35-2 is a valid CAS Registry Number.

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1269662-35-2Relevant academic research and scientific papers

Tin (IV) chloride-promoted one-pot synthesis of novel tacrine analogues

Hu, Huanan,Song, Liangfu,Fang, Qianqian,Zheng, Junjun,Meng, Zhiwei,Luo, Yiting

experimental part, p. 1878 - 1887 (2011/04/22)

A facile synthesis of potential acetylcholinesterase (AChE) inhibitors, the tacrine analogues 3a-p, has been accomplished by direct cyclocondensation of 1-aryl-4- cyano-5-aminopyrazole with β-ketoesters using tin(IV) chloride as catalyst. The structures o

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