Cas 100592-85-6,(7-Methyl-2-methylsulfanyl-pyrazolo[1,5-a]pyridin-3-yl)-phenyl-methanone

100592-85-6

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Basic information

Product Name: (7-Methyl-2-methylsulfanyl-pyrazolo[1,5-a]pyridin-3-yl)-phenyl-methanone
Synonyms: (7-Methyl-2-methylsulfanyl-pyrazolo[1,5-a]pyridin-3-yl)-phenyl-methanone
CAS NO:100592-85-6
Molecular Formula:
Molecular Weight: 282.366
EINECS: N/A
Product Categories: N/A
Mol File: 100592-85-6.mol
Article Data: 1

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: (7-Methyl-2-methylsulfanyl-pyrazolo[1,5-a]pyridin-3-yl)-phenyl-methanone(CAS DataBase Reference)
NIST Chemistry Reference: (7-Methyl-2-methylsulfanyl-pyrazolo[1,5-a]pyridin-3-yl)-phenyl-methanone(100592-85-6)
EPA Substance Registry System: (7-Methyl-2-methylsulfanyl-pyrazolo[1,5-a]pyridin-3-yl)-phenyl-methanone(100592-85-6)

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: 100592-85-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 100592-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,9 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100592-85:
(8*1)+(7*0)+(6*0)+(5*5)+(4*9)+(3*2)+(2*8)+(1*5)=96
96 % 10 = 6
So 100592-85-6 is a valid CAS Registry Number.

100592-85-6Upstream product

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100592-85-6Relevant articles and documents

Preparation of New Nitrogen-bridged Heterocycles. 11. A New Synthetic Method of Pyrazolopyridines from the Alkaline Treatment of 1-pyridinium Salts

Kakehi, Akikazu,Ito, Suketaka,Ito, Masayoshi,Yotsuya, Toshiaki,Nagata, Kenji

, p. 1432 - 1442 (2007/10/02)

Alkaline treatment of 1-pyridinium halides gave unexpectedly 3-acyl- or 3-(acylthio)pyrazolopyridine derivatives in 35-87percent yields.Some 4,4a-dihydropyridothiadiazine intermediates involved in these

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