Cas 936338-94-2,ethyl 1-benzoyl-3-(2-cyanoethylthio)thieno[3,4-b]indolizine-9-carboxylate

936338-94-2

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Basic information

Product Name: ethyl 1-benzoyl-3-(2-cyanoethylthio)thieno[3,4-b]indolizine-9-carboxylate
Synonyms: ethyl 1-benzoyl-3-(2-cyanoethylthio)thieno[3,4-b]indolizine-9-carboxylate
CAS NO:936338-94-2
Molecular Formula:
Molecular Weight: 434.54
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: ethyl 1-benzoyl-3-(2-cyanoethylthio)thieno[3,4-b]indolizine-9-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 1-benzoyl-3-(2-cyanoethylthio)thieno[3,4-b]indolizine-9-carboxylate(936338-94-2)
EPA Substance Registry System: ethyl 1-benzoyl-3-(2-cyanoethylthio)thieno[3,4-b]indolizine-9-carboxylate(936338-94-2)

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: 936338-94-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 936338-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,3,3 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 936338-94:
(8*9)+(7*3)+(6*6)+(5*3)+(4*3)+(3*8)+(2*9)+(1*4)=202
202 % 10 = 2
So 936338-94-2 is a valid CAS Registry Number.

936338-94-2Upstream product

433211-61-1 C₂₀H₁₇NO₃S₂

936338-94-2Downstream Products

936338-94-2Relevant academic research and scientific papers

Preparation of new nitrogen-bridged heterocycles. 59.1) syntheses and intramolecular interactions of 3-(acylmethylthio)- and 3-[(3-ethoxycarbonyl-2-propenyl)thio]thieno[3,4-b]indolizine derivatives

Kakehi, Akikazu,Suga, Hiroyuki,Isogai, Hirohide

, p. 95 - 101 (2007)

Various thieno[3,4-b]indolizine derivatives having an acylmethylthio or (3-ethoxycarbonyl-2-propenyl)thio group at the 3-position which could not be obtained by a conventional method were prepared by a new procedure using cyanoethyl group as a protecting

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