Cas 656258-19-4,2-Thiazolamine, 5-[2-[4-[(5-methyl-3-isoxazolyl)methoxy]phenyl]-4-pyridinyl]-4-(6-methyl- 2-pyridinyl)-

656258-19-4

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Basic information

Product Name: 2-Thiazolamine, 5-[2-[4-[(5-methyl-3-isoxazolyl)methoxy]phenyl]-4-pyridinyl]-4-(6-methyl- 2-pyridinyl)-
Synonyms:
CAS NO:656258-19-4
Molecular Formula: C25H21N5O2S
Molecular Weight: 455.54
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: 2-Thiazolamine, 5-[2-[4-[(5-methyl-3-isoxazolyl)methoxy]phenyl]-4-pyridinyl]-4-(6-methyl- 2-pyridinyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Thiazolamine, 5-[2-[4-[(5-methyl-3-isoxazolyl)methoxy]phenyl]-4-pyridinyl]-4-(6-methyl- 2-pyridinyl)-(656258-19-4)
EPA Substance Registry System: 2-Thiazolamine, 5-[2-[4-[(5-methyl-3-isoxazolyl)methoxy]phenyl]-4-pyridinyl]-4-(6-methyl- 2-pyridinyl)-(656258-19-4)

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: 656258-19-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 656258-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,6,2,5 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 656258-19:
(8*6)+(7*5)+(6*6)+(5*2)+(4*5)+(3*8)+(2*1)+(1*9)=184
184 % 10 = 4
So 656258-19-4 is a valid CAS Registry Number.

656258-19-4Upstream product

35166-37-1 3-chloromethyl-5-methylisoxazole

656258-19-4Downstream Products

656258-19-4Relevant academic research and scientific papers

2-PHENYLPYRIDIN-4-YL DERIVATIVES AS ALK5 INHIBITORS

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Page 105, (2010/02/06)

This invention relates to novel 2-phenylpyridin-4-yl heterocyclyl derivatives which are inhibitors of the transforming growth factor, ("TGF")-? signalling pathway, in particular, the phosphorylation of smad2 or smad3 by the TGF-β type I or activin-like kinase ("ALK")-5 receptor, methods for their preparation and their use in medicine, specifically in the treatment and prevention of a disease state mediated by this pathway.

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