Cas 1117686-32-4,N-[2-(4,4-difluoropiperidin-1-yl)ethyl]-4-{[4-(2,6-dimethyl-pyridin-3-yl)oxypyridin-2-yl]amino}benzamide

1117686-32-4

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Basic information

Product Name: N-[2-(4,4-difluoropiperidin-1-yl)ethyl]-4-{[4-(2,6-dimethyl-pyridin-3-yl)oxypyridin-2-yl]amino}benzamide
Synonyms: N-[2-(4,4-difluoropiperidin-1-yl)ethyl]-4-{[4-(2,6-dimethyl-pyridin-3-yl)oxypyridin-2-yl]amino}benzamide
CAS NO:1117686-32-4
Molecular Formula:
Molecular Weight: 481.545
EINECS: N/A
Product Categories: N/A
Mol File: 1117686-32-4.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: N-[2-(4,4-difluoropiperidin-1-yl)ethyl]-4-{[4-(2,6-dimethyl-pyridin-3-yl)oxypyridin-2-yl]amino}benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[2-(4,4-difluoropiperidin-1-yl)ethyl]-4-{[4-(2,6-dimethyl-pyridin-3-yl)oxypyridin-2-yl]amino}benzamide(1117686-32-4)
EPA Substance Registry System: N-[2-(4,4-difluoropiperidin-1-yl)ethyl]-4-{[4-(2,6-dimethyl-pyridin-3-yl)oxypyridin-2-yl]amino}benzamide(1117686-32-4)

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: 1117686-32-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1117686-32-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,7,6,8 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1117686-32:
(9*1)+(8*1)+(7*1)+(6*7)+(5*6)+(4*8)+(3*6)+(2*3)+(1*2)=154
154 % 10 = 4
So 1117686-32-4 is a valid CAS Registry Number.

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1117686-32-4Relevant articles and documents

CHEMICAL COMPOUNDS-821

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Page/Page column 60, (2009/03/07)

The invention relates to chemical compounds of the formula (I), or pharmaceutically acceptable salts thereof, which possess ALK5 (TGFβR1) inhibitory activity and are accordingly useful for their anti-cancer activity and thus in methods of treatment of the

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