Cas 91742-81-3,1-[2-(diethylamino)ethyl]-2-(4-ethoxybenzyl)-5-(methylfumaramido)benzimidazole

91742-81-3

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Basic information

Product Name: 1-[2-(diethylamino)ethyl]-2-(4-ethoxybenzyl)-5-(methylfumaramido)benzimidazole
Synonyms: 1-[2-(diethylamino)ethyl]-2-(4-ethoxybenzyl)-5-(methylfumaramido)benzimidazole
CAS NO:91742-81-3
Molecular Formula:
Molecular Weight: 478.591
EINECS: N/A
Product Categories: N/A
Mol File: 91742-81-3.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: 1-[2-(diethylamino)ethyl]-2-(4-ethoxybenzyl)-5-(methylfumaramido)benzimidazole(CAS DataBase Reference)
NIST Chemistry Reference: 1-[2-(diethylamino)ethyl]-2-(4-ethoxybenzyl)-5-(methylfumaramido)benzimidazole(91742-81-3)
EPA Substance Registry System: 1-[2-(diethylamino)ethyl]-2-(4-ethoxybenzyl)-5-(methylfumaramido)benzimidazole(91742-81-3)

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: 91742-81-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91742-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,4 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91742-81:
(7*9)+(6*1)+(5*7)+(4*4)+(3*2)+(2*8)+(1*1)=143
143 % 10 = 3
So 91742-81-3 is a valid CAS Registry Number.

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91742-81-3Relevant articles and documents

Probes for narcotic receptor mediated phenomena. 7. Synthesis and pharmacological properties of irreversible ligands specific for μ or δ opiate receptors

Burke Jr.,Bajwa,Jacobson,Rice,Streaty,Klee

, p. 1570 - 1574 (2007/10/02)

Syntheses of affinity reagents for opiate receptors based on the fentanyl, endo-ethenotetrahydrooripavine, and etonitazene carbon-nitrogen skeletons are described. The isothiocyanate, bromoacetamido, and methylfumaramido alkylating functions were employed

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