Cas 406679-38-7,4-chloro-N-((5-(4-oxopiperidin-1-ylsulfonyl)thiophen-2-yl)methyl)benzamide

406679-38-7

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Basic information

Product Name: 4-chloro-N-((5-(4-oxopiperidin-1-ylsulfonyl)thiophen-2-yl)methyl)benzamide
Synonyms: 4-chloro-N-((5-(4-oxopiperidin-1-ylsulfonyl)thiophen-2-yl)methyl)benzamide;4-chloro-N-{[5-(4-oxopiperidine-1-sulfonyl)thiophen-2-yl]Methyl}benzaMide
CAS NO:406679-38-7
Molecular Formula: C17H17ClN2O4S2
Molecular Weight: 413
EINECS: N/A
Product Categories: N/A
Mol File: 406679-38-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-chloro-N-((5-(4-oxopiperidin-1-ylsulfonyl)thiophen-2-yl)methyl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-chloro-N-((5-(4-oxopiperidin-1-ylsulfonyl)thiophen-2-yl)methyl)benzamide(406679-38-7)
EPA Substance Registry System: 4-chloro-N-((5-(4-oxopiperidin-1-ylsulfonyl)thiophen-2-yl)methyl)benzamide(406679-38-7)

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: 406679-38-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 406679-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,6,7 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 406679-38:
(8*4)+(7*0)+(6*6)+(5*6)+(4*7)+(3*9)+(2*3)+(1*8)=167
167 % 10 = 7
So 406679-38-7 is a valid CAS Registry Number.

406679-38-7Upstream product

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406679-38-7Relevant academic research and scientific papers

Pharmaceutically active sulfonamide derivatives bearing both lipophilic and ionisable moieties as inhibitors of protein Junkinases

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Page 17, (2008/06/13)

The present invention is related to sulfonamide derivatives having a lipophilic moiety and which are substantially soluble under physiological conditions. Said compounds are notably for use as pharmaceutically active compounds. The present invention also

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