Cas 75184-12-2,4-Ethylsulfanyl-2-oxo-10-phenyl-2H-pyrano[2,3-b]indolizine-3-carboxylic acid ethyl ester

75184-12-2

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Basic information

Product Name: 4-Ethylsulfanyl-2-oxo-10-phenyl-2H-pyrano[2,3-b]indolizine-3-carboxylic acid ethyl ester
Synonyms: 4-Ethylsulfanyl-2-oxo-10-phenyl-2H-pyrano[2,3-b]indolizine-3-carboxylic acid ethyl ester
CAS NO:75184-12-2
Molecular Formula:
Molecular Weight: 393.463
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: 4-Ethylsulfanyl-2-oxo-10-phenyl-2H-pyrano[2,3-b]indolizine-3-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Ethylsulfanyl-2-oxo-10-phenyl-2H-pyrano[2,3-b]indolizine-3-carboxylic acid ethyl ester(75184-12-2)
EPA Substance Registry System: 4-Ethylsulfanyl-2-oxo-10-phenyl-2H-pyrano[2,3-b]indolizine-3-carboxylic acid ethyl ester(75184-12-2)

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: 75184-12-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75184-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,8 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75184-12:
(7*7)+(6*5)+(5*1)+(4*8)+(3*4)+(2*1)+(1*2)=132
132 % 10 = 2
So 75184-12-2 is a valid CAS Registry Number.

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75184-12-2Relevant academic research and scientific papers

Preparation of New Nitrogen-bridged Heterocycles. A Facile Synthetic Method of Pyranoindolizinone Derivatives

Kakehi, Akikazu,Ito, Suketaka,Nakanishi, Kazunori,Watanabe, Kozo,Kitagawa, Masahiko

, p. 1115 - 1120 (2007/10/02)

Pyranoindolizinone derivatives were formed in 18-98 percent yields by the reactions of 3-bis(alkylthio)-methylene)-2,3-dihydroindolizin-2-ones with various acetates in the presence of alkali.Dihydroindolizinones were readily obtained by the alkali

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