Cas 88121-64-6,(3aR,9aS,9bS)-1,3-Dioxo-2-p-tolyl-1,2,3,3a,9a,9b-hexahydro-pyrrolo[3,4-a]indolizine-4,4-dicarboxylic acid diethyl ester

88121-64-6

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Basic information

Product Name: (3aR,9aS,9bS)-1,3-Dioxo-2-p-tolyl-1,2,3,3a,9a,9b-hexahydro-pyrrolo[3,4-a]indolizine-4,4-dicarboxylic acid diethyl ester
Synonyms: (3aR,9aS,9bS)-1,3-Dioxo-2-p-tolyl-1,2,3,3a,9a,9b-hexahydro-pyrrolo[3,4-a]indolizine-4,4-dicarboxylic acid diethyl ester
CAS NO:88121-64-6
Molecular Formula:
Molecular Weight: 424.453
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: (3aR,9aS,9bS)-1,3-Dioxo-2-p-tolyl-1,2,3,3a,9a,9b-hexahydro-pyrrolo[3,4-a]indolizine-4,4-dicarboxylic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,9aS,9bS)-1,3-Dioxo-2-p-tolyl-1,2,3,3a,9a,9b-hexahydro-pyrrolo[3,4-a]indolizine-4,4-dicarboxylic acid diethyl ester(88121-64-6)
EPA Substance Registry System: (3aR,9aS,9bS)-1,3-Dioxo-2-p-tolyl-1,2,3,3a,9a,9b-hexahydro-pyrrolo[3,4-a]indolizine-4,4-dicarboxylic acid diethyl ester(88121-64-6)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 88121-64-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88121-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,2 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88121-64:
(7*8)+(6*8)+(5*1)+(4*2)+(3*1)+(2*6)+(1*4)=136
136 % 10 = 6
So 88121-64-6 is a valid CAS Registry Number.

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88121-64-6Relevant academic research and scientific papers

STEREOSELECTIVE CYCLOADDITION REACTION OF PYRIDINIUM AND THIAZOLIUM METHYLIDES TO ELECTRON-DEFICIENT OLEFINIC DIPOLAROPHILES

Tsuge, Otohiko,Kanemasa, Shuji,Takenaka, Shigeori

, p. 1907 - 1912 (2007/10/02)

The cycloaddition reaction of pyridinium and thiazolium methylides to electron-deficient olefinic dipolarophiles has been found to take place through an endo approach of the anti-ylides to the dipolarophiles affording the stereoselective cycloaddu

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