Cas 847448-71-9,tert-butyl 3-[5-(1-tert-butoxycarbonyl-1H-indole-3-carbonyl)-1-ethoxymethyl-4-phenyl-1H-imidazole-2-carbonyl]indole-1-carboxylate

847448-71-9

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Basic information

Product Name: tert-butyl 3-[5-(1-tert-butoxycarbonyl-1H-indole-3-carbonyl)-1-ethoxymethyl-4-phenyl-1H-imidazole-2-carbonyl]indole-1-carboxylate
Synonyms: tert-butyl 3-[5-(1-tert-butoxycarbonyl-1H-indole-3-carbonyl)-1-ethoxymethyl-4-phenyl-1H-imidazole-2-carbonyl]indole-1-carboxylate
CAS NO:847448-71-9
Molecular Formula:
Molecular Weight: 688.78
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: tert-butyl 3-[5-(1-tert-butoxycarbonyl-1H-indole-3-carbonyl)-1-ethoxymethyl-4-phenyl-1H-imidazole-2-carbonyl]indole-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 3-[5-(1-tert-butoxycarbonyl-1H-indole-3-carbonyl)-1-ethoxymethyl-4-phenyl-1H-imidazole-2-carbonyl]indole-1-carboxylate(847448-71-9)
EPA Substance Registry System: tert-butyl 3-[5-(1-tert-butoxycarbonyl-1H-indole-3-carbonyl)-1-ethoxymethyl-4-phenyl-1H-imidazole-2-carbonyl]indole-1-carboxylate(847448-71-9)

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: 847448-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 847448-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,4,4 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 847448-71:
(8*8)+(7*4)+(6*7)+(5*4)+(4*4)+(3*8)+(2*7)+(1*1)=209
209 % 10 = 9
So 847448-71-9 is a valid CAS Registry Number.

847448-71-9Upstream product

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847448-71-9Relevant academic research and scientific papers

Synthesis of homocarbonyltopsentine derivatives

Montagne, Cyril,Fournet, Guy,Joseph, Benoit

, p. 136 - 146 (2005)

Homocarbonyltopsentines I are known to exhibit interesting anti-inflammatory activity in vivo. In order to study the role of the heterocycles in the modulation of their activity, several analogues in which indoles were replaced either by substituted indol

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