Cas 1279575-79-9,(1S,4R,5S)-1'-tert-butyl 3,5-dimethyl 4-(4-chlorophenyl)-2'-oxospiro[cyclopent[2]ene-1,3'-indoline]-1',3,5-tricarboxylate

1279575-79-9

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Basic information

Product Name: (1S,4R,5S)-1'-tert-butyl 3,5-dimethyl 4-(4-chlorophenyl)-2'-oxospiro[cyclopent[2]ene-1,3'-indoline]-1',3,5-tricarboxylate
Synonyms: (1S,4R,5S)-1'-tert-butyl 3,5-dimethyl 4-(4-chlorophenyl)-2'-oxospiro[cyclopent[2]ene-1,3'-indoline]-1',3,5-tricarboxylate
CAS NO:1279575-79-9
Molecular Formula:
Molecular Weight: 511.959
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,4R,5S)-1'-tert-butyl 3,5-dimethyl 4-(4-chlorophenyl)-2'-oxospiro[cyclopent[2]ene-1,3'-indoline]-1',3,5-tricarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,4R,5S)-1'-tert-butyl 3,5-dimethyl 4-(4-chlorophenyl)-2'-oxospiro[cyclopent[2]ene-1,3'-indoline]-1',3,5-tricarboxylate(1279575-79-9)
EPA Substance Registry System: (1S,4R,5S)-1'-tert-butyl 3,5-dimethyl 4-(4-chlorophenyl)-2'-oxospiro[cyclopent[2]ene-1,3'-indoline]-1',3,5-tricarboxylate(1279575-79-9)

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: 1279575-79-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1279575-79-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,5,7 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1279575-79:
(9*1)+(8*2)+(7*7)+(6*9)+(5*5)+(4*7)+(3*5)+(2*7)+(1*9)=219
219 % 10 = 9
So 1279575-79-9 is a valid CAS Registry Number.

1279575-79-9Upstream product

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1279575-79-9Relevant academic research and scientific papers

Core-structure-motivated design of a phosphine-catalyzed [3 + 2] cycloaddition reaction: Enantioselective syntheses of spirocyclopenteneoxindoles

Tan, Bin,Candeias, Nuno R.,Barbas, Carlos F.

, p. 4672 - 4675 (2011/06/19)

A novel organocatalytic asymmetric [3 + 2] cycloaddition reaction between methyleneindolinones and allylic compounds yielding complex spirocyclopentaneoxindoles has been developed. It provides extraordinary levels of enantioselective control involving a c

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