Cas 144633-19-2,1H-4,10a-Epithiopyrrolo[3,4-a]quinolizine-1,3,5(2H,4H)-trione, hexahydro-10-methyl-10-(4-pentenyl)-2-phenyl-

144633-19-2

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Basic information

Product Name: 1H-4,10a-Epithiopyrrolo[3,4-a]quinolizine-1,3,5(2H,4H)-trione, hexahydro-10-methyl-10-(4-pentenyl)-2-phenyl-
Synonyms:
CAS NO:144633-19-2
Molecular Formula: C23H26N2O3S
Molecular Weight: 410.537
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: 1H-4,10a-Epithiopyrrolo[3,4-a]quinolizine-1,3,5(2H,4H)-trione, hexahydro-10-methyl-10-(4-pentenyl)-2-phenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-4,10a-Epithiopyrrolo[3,4-a]quinolizine-1,3,5(2H,4H)-trione, hexahydro-10-methyl-10-(4-pentenyl)-2-phenyl-(144633-19-2)
EPA Substance Registry System: 1H-4,10a-Epithiopyrrolo[3,4-a]quinolizine-1,3,5(2H,4H)-trione, hexahydro-10-methyl-10-(4-pentenyl)-2-phenyl-(144633-19-2)

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: 144633-19-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144633-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,6,3 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144633-19:
(8*1)+(7*4)+(6*4)+(5*6)+(4*3)+(3*3)+(2*1)+(1*9)=122
122 % 10 = 2
So 144633-19-2 is a valid CAS Registry Number.

144633-19-2Upstream product

144633-19-2Downstream Products

144633-19-2Relevant academic research and scientific papers

Generation and cycloaddition reactions of transient alkyl-substituted anhydro-4-hydroxythiazolium hydroxides

Hertzog, Donald L.,Nadler, William R.,Zhang, Zhijia J.,Padwa, Albert

, p. 5877 - 5880 (1992)

Transient alkyl-substituted anhydro-4-hydroxythiazolium hydroxides undergo efficient inter- and intramolecular cycloaddition to provide the corresponding 1,3-dipolar cycloadducts in high yield.

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