Cas 117523-70-3,N-(6-Chloro-pyrimidin-4-yl)-2-methoxy-N-(1-phenethyl-piperidin-4-yl)-acetamide

117523-70-3

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Basic information

Product Name: N-(6-Chloro-pyrimidin-4-yl)-2-methoxy-N-(1-phenethyl-piperidin-4-yl)-acetamide
Synonyms: N-(6-Chloro-pyrimidin-4-yl)-2-methoxy-N-(1-phenethyl-piperidin-4-yl)-acetamide
CAS NO:117523-70-3
Molecular Formula:
Molecular Weight: 388.897
EINECS: N/A
Product Categories: N/A
Mol File: 117523-70-3.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-(6-Chloro-pyrimidin-4-yl)-2-methoxy-N-(1-phenethyl-piperidin-4-yl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(6-Chloro-pyrimidin-4-yl)-2-methoxy-N-(1-phenethyl-piperidin-4-yl)-acetamide(117523-70-3)
EPA Substance Registry System: N-(6-Chloro-pyrimidin-4-yl)-2-methoxy-N-(1-phenethyl-piperidin-4-yl)-acetamide(117523-70-3)

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: 117523-70-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 117523-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,5,2 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117523-70:
(8*1)+(7*1)+(6*7)+(5*5)+(4*2)+(3*3)+(2*7)+(1*0)=113
113 % 10 = 3
So 117523-70-3 is a valid CAS Registry Number.

117523-70-3Upstream product

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117523-70-3Relevant articles and documents

New 4-(heteroanilido)piperidines, structurally related to the pure opioid agonist fentanyl, with agonist and/or antagonist properties

Bagley,Wynn,Rudo,Doorley,Spencer,Spaulding

, p. 663 - 671 (2007/10/02)

A research program based on certain heterocyclic modifications (12-50) of the fentanyl (1) molecule has generated a novel class of opioids. In the mouse hot-place test, these compounds were weaker analgesics than 1. Two types of antagonists were observed

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