Cas 133601-82-8,(1S,8aR)-1-(4-Chloro-benzoyl)-5-(4-chloro-phenyl)-3-phenyl-8,8a-dihydro-1H-[1,4]thiazino[3,4,5-cd]indolizin-4-one

133601-82-8

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Basic information

Product Name: (1S,8aR)-1-(4-Chloro-benzoyl)-5-(4-chloro-phenyl)-3-phenyl-8,8a-dihydro-1H-[1,4]thiazino[3,4,5-cd]indolizin-4-one
Synonyms: (1S,8aR)-1-(4-Chloro-benzoyl)-5-(4-chloro-phenyl)-3-phenyl-8,8a-dihydro-1H-[1,4]thiazino[3,4,5-cd]indolizin-4-one
CAS NO:133601-82-8
Molecular Formula:
Molecular Weight: 516.447
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: (1S,8aR)-1-(4-Chloro-benzoyl)-5-(4-chloro-phenyl)-3-phenyl-8,8a-dihydro-1H-[1,4]thiazino[3,4,5-cd]indolizin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (1S,8aR)-1-(4-Chloro-benzoyl)-5-(4-chloro-phenyl)-3-phenyl-8,8a-dihydro-1H-[1,4]thiazino[3,4,5-cd]indolizin-4-one(133601-82-8)
EPA Substance Registry System: (1S,8aR)-1-(4-Chloro-benzoyl)-5-(4-chloro-phenyl)-3-phenyl-8,8a-dihydro-1H-[1,4]thiazino[3,4,5-cd]indolizin-4-one(133601-82-8)

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: 133601-82-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133601-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,0 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133601-82:
(8*1)+(7*3)+(6*3)+(5*6)+(4*0)+(3*1)+(2*8)+(1*2)=98
98 % 10 = 8
So 133601-82-8 is a valid CAS Registry Number.

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133601-82-8Relevant academic research and scientific papers

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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