Cas 107453-95-2,8-{[1-(4-Benzhydryl-piperidin-1-yl)-meth-(E)-ylidene]-amino}-octanoic acid 2,2,2-trichloro-ethyl ester

107453-95-2

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Basic information

Product Name: 8-{[1-(4-Benzhydryl-piperidin-1-yl)-meth-(E)-ylidene]-amino}-octanoic acid 2,2,2-trichloro-ethyl ester
Synonyms:
CAS NO:107453-95-2
Molecular Formula:
Molecular Weight: 551.984
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: 8-{[1-(4-Benzhydryl-piperidin-1-yl)-meth-(E)-ylidene]-amino}-octanoic acid 2,2,2-trichloro-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 8-{[1-(4-Benzhydryl-piperidin-1-yl)-meth-(E)-ylidene]-amino}-octanoic acid 2,2,2-trichloro-ethyl ester(107453-95-2)
EPA Substance Registry System: 8-{[1-(4-Benzhydryl-piperidin-1-yl)-meth-(E)-ylidene]-amino}-octanoic acid 2,2,2-trichloro-ethyl ester(107453-95-2)

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: 107453-95-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107453-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,5 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107453-95:
(8*1)+(7*0)+(6*7)+(5*4)+(4*5)+(3*3)+(2*9)+(1*5)=122
122 % 10 = 2
So 107453-95-2 is a valid CAS Registry Number.

107453-95-2Upstream product

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107453-95-2Relevant academic research and scientific papers

Antisecretory Activity of Human, Dog, and Rat Metabolites of Fenoctimine

Scott, Malcolm K.,Jacoby, Henry, I.,Bonfilio, Antoinette, C.,Corcoran, Thomas W.,Lopez, Iris S.

, p. 894 - 899 (2007/10/02)

Fenoctimine (1a), a nonanticholinergic inhibitor of gastric acid secretion in dogs and rats, was evaluated as a gastric antisecretory agent in humans.In humans it exhibited weak antisecretory activity and caused anticholinergic-like side effects such as d

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