Cas 1333429-79-0,(2S,3S,4S)-tert-butyl 6-chloro-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate

1333429-79-0

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Basic information

Product Name: (2S,3S,4S)-tert-butyl 6-chloro-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate
Synonyms: (2S,3S,4S)-tert-butyl 6-chloro-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate
CAS NO:1333429-79-0
Molecular Formula:
Molecular Weight: 468.937
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 6-chloro-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,4S)-tert-butyl 6-chloro-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate(1333429-79-0)
EPA Substance Registry System: (2S,3S,4S)-tert-butyl 6-chloro-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate(1333429-79-0)

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: 1333429-79-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1333429-79-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,4,2 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1333429-79:
(9*1)+(8*3)+(7*3)+(6*3)+(5*4)+(4*2)+(3*9)+(2*7)+(1*9)=150
150 % 10 = 0
So 1333429-79-0 is a valid CAS Registry Number.

1333429-79-0Upstream product

1333429-79-0Downstream Products

1333430-04-8 C₂₅H₂₇ClN₂O₅

1333429-79-0Relevant 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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