Cas 1210071-85-4,ethyl 1'-acetyl-4-hydroxy-2-(4-(methoxycarbonyl)phenyl)-2'-oxo-6-phenylspiro[cyclohex[3]ene-1,3'-indoline]-3-carboxylate

1210071-85-4

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Basic information

Product Name: ethyl 1'-acetyl-4-hydroxy-2-(4-(methoxycarbonyl)phenyl)-2'-oxo-6-phenylspiro[cyclohex[3]ene-1,3'-indoline]-3-carboxylate
Synonyms:
CAS NO:1210071-85-4
Molecular Formula:
Molecular Weight: 539.585
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 1'-acetyl-4-hydroxy-2-(4-(methoxycarbonyl)phenyl)-2'-oxo-6-phenylspiro[cyclohex[3]ene-1,3'-indoline]-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 1'-acetyl-4-hydroxy-2-(4-(methoxycarbonyl)phenyl)-2'-oxo-6-phenylspiro[cyclohex[3]ene-1,3'-indoline]-3-carboxylate(1210071-85-4)
EPA Substance Registry System: ethyl 1'-acetyl-4-hydroxy-2-(4-(methoxycarbonyl)phenyl)-2'-oxo-6-phenylspiro[cyclohex[3]ene-1,3'-indoline]-3-carboxylate(1210071-85-4)

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: 1210071-85-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1210071-85-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,0,0,7 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1210071-85:
(9*1)+(8*2)+(7*1)+(6*0)+(5*0)+(4*7)+(3*1)+(2*8)+(1*5)=84
84 % 10 = 4
So 1210071-85-4 is a valid CAS Registry Number.

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1210071-85-4Relevant academic research and scientific papers

Organocatalytic asymmetric formal [4 + 2] cycloaddition for the synthesis of spiro[4-eyelohexanone-1,3′-oxindoline] derivatives in high optical purity

Wei, Qiang,Gong, Liu-Zhu

, p. 1008 - 1011 (2010)

Chemical Equetion Presentation A bifunctional organocatalytic asymmetric formal [4 + 2] cycloaddition reaction of Nazarov reagents and methyleneindolinones afforded spiro[4-cyclohexanone-1,3′-oxindoline] derivatives with excellent enantioselectivity (up to 98% ee).

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