Cas 1333430-41-3,(2S,3S,4S)-tert-butyl 2-(4-bromobenzoyl)-2'-oxo-4-(2-oxoethyl)-1,2-dihydrospiro[carbazole-3,3'-indoline]-9(4H)-carboxylate

1333430-41-3

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Basic information

Product Name: (2S,3S,4S)-tert-butyl 2-(4-bromobenzoyl)-2'-oxo-4-(2-oxoethyl)-1,2-dihydrospiro[carbazole-3,3'-indoline]-9(4H)-carboxylate
Synonyms: (2S,3S,4S)-tert-butyl 2-(4-bromobenzoyl)-2'-oxo-4-(2-oxoethyl)-1,2-dihydrospiro[carbazole-3,3'-indoline]-9(4H)-carboxylate
CAS NO:1333430-41-3
Molecular Formula:
Molecular Weight: 613.508
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: (2S,3S,4S)-tert-butyl 2-(4-bromobenzoyl)-2'-oxo-4-(2-oxoethyl)-1,2-dihydrospiro[carbazole-3,3'-indoline]-9(4H)-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,4S)-tert-butyl 2-(4-bromobenzoyl)-2'-oxo-4-(2-oxoethyl)-1,2-dihydrospiro[carbazole-3,3'-indoline]-9(4H)-carboxylate(1333430-41-3)
EPA Substance Registry System: (2S,3S,4S)-tert-butyl 2-(4-bromobenzoyl)-2'-oxo-4-(2-oxoethyl)-1,2-dihydrospiro[carbazole-3,3'-indoline]-9(4H)-carboxylate(1333430-41-3)

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: 1333430-41-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1333430-41-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,4,3 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1333430-41:
(9*1)+(8*3)+(7*3)+(6*3)+(5*4)+(4*3)+(3*0)+(2*4)+(1*1)=113
113 % 10 = 3
So 1333430-41-3 is a valid CAS Registry Number.

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1333430-41-3Relevant academic research and scientific papers

Asymmetric catalysis of Diels-Alder reactions with in situ generated heterocyclic ortho -quinodimethanes

Liu, Yankai,Nappi, Manuel,Arceo, Elena,Vera, Silvia,Melchiorre, Paolo

, p. 15212 - 15218 (2011/11/13)

The Diels-Alder reaction is probably the most powerful technology in the synthetic repertoire for single-step constructions of complex chiral molecules. The synthetic power of this fundamental pericyclic transformation has greatly increased with the emerg

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