Cas 1309883-46-2,ethyl (2R,6R)-2',4-dioxo-2,6-di-p-tolylspiro[cyclohexane-1,3'-indoline]-1'-carboxylate

1309883-46-2

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Basic information

Product Name: ethyl (2R,6R)-2',4-dioxo-2,6-di-p-tolylspiro[cyclohexane-1,3'-indoline]-1'-carboxylate
Synonyms: ethyl (2R,6R)-2',4-dioxo-2,6-di-p-tolylspiro[cyclohexane-1,3'-indoline]-1'-carboxylate
CAS NO:1309883-46-2
Molecular Formula:
Molecular Weight: 467.565
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: ethyl (2R,6R)-2',4-dioxo-2,6-di-p-tolylspiro[cyclohexane-1,3'-indoline]-1'-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (2R,6R)-2',4-dioxo-2,6-di-p-tolylspiro[cyclohexane-1,3'-indoline]-1'-carboxylate(1309883-46-2)
EPA Substance Registry System: ethyl (2R,6R)-2',4-dioxo-2,6-di-p-tolylspiro[cyclohexane-1,3'-indoline]-1'-carboxylate(1309883-46-2)

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: 1309883-46-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1309883-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,8,8 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1309883-46:
(9*1)+(8*3)+(7*0)+(6*9)+(5*8)+(4*8)+(3*3)+(2*4)+(1*6)=182
182 % 10 = 2
So 1309883-46-2 is a valid CAS Registry Number.

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1309883-46-2Relevant academic research and scientific papers

A highly organocatalytic stereoselective double Michael reaction: Efficient construction of optically enriched spirocyclic oxindoles

Wang, Liang-Liang,Peng, Lin,Bai, Jian-Fei,Jia, Li-Na,Luo, Xi-Ya,Huang, Qing-Chun,Xu, Xiao-Ying,Wang, Li-Xin

supporting information; experimental part, p. 5593 - 5595 (2011/06/21)

An effective double Michael reaction has been disclosed to access spirocyclic oxindoles in high yields (up to 98%) and excellent enantioselectivities (up to 98% ee).

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