Cas 133328-76-4,(1R,8aR)-5-Methyl-4-oxo-3-phenyl-1,4,8,8a-tetrahydro-[1,4]thiazino[3,4,5-cd]indolizine-1-carboxylic acid ethyl ester

133328-76-4

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Basic information

Product Name: (1R,8aR)-5-Methyl-4-oxo-3-phenyl-1,4,8,8a-tetrahydro-[1,4]thiazino[3,4,5-cd]indolizine-1-carboxylic acid ethyl ester
Synonyms:
CAS NO:133328-76-4
Molecular Formula:
Molecular Weight: 353.442
EINECS: N/A
Product Categories: N/A
Mol File: 133328-76-4.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: (1R,8aR)-5-Methyl-4-oxo-3-phenyl-1,4,8,8a-tetrahydro-[1,4]thiazino[3,4,5-cd]indolizine-1-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1R,8aR)-5-Methyl-4-oxo-3-phenyl-1,4,8,8a-tetrahydro-[1,4]thiazino[3,4,5-cd]indolizine-1-carboxylic acid ethyl ester(133328-76-4)
EPA Substance Registry System: (1R,8aR)-5-Methyl-4-oxo-3-phenyl-1,4,8,8a-tetrahydro-[1,4]thiazino[3,4,5-cd]indolizine-1-carboxylic acid ethyl ester(133328-76-4)

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: 133328-76-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133328-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,2 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133328-76:
(8*1)+(7*3)+(6*3)+(5*3)+(4*2)+(3*8)+(2*7)+(1*6)=114
114 % 10 = 4
So 133328-76-4 is a valid CAS Registry Number.

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133328-76-4Relevant articles and documents

Preparation of New Nitrogen-Bridged Heterocycles. 25. A Smooth Synthesis of Thiazinoindolizine Derivatives

Kakehi, Akikazu,Ito, Suketaka,Fujii, Tsuneo,Sakurai, Tosio,Urushido, Kunio,et al.

, p. 3571 - 3578 (2007/10/02)

The title compounds were prepared smoothly in moderate yields by the reactions of 3-(mercaptomethylene)-2(3H)-indolizinones with various alkylating agents such as bromoacetonitrile, bromoacetates, and phenacyl bromides in the presence of base.The structur

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