Cas 342376-59-4,(Z)-2-(Benzhydrylidene-amino)-pent-2-enedioic acid 1-tert-butyl ester 5-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl] ester

342376-59-4

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Basic information

Product Name: (Z)-2-(Benzhydrylidene-amino)-pent-2-enedioic acid 1-tert-butyl ester 5-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl] ester
Synonyms: (Z)-2-(Benzhydrylidene-amino)-pent-2-enedioic acid 1-tert-butyl ester 5-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl] ester
CAS NO:342376-59-4
Molecular Formula:
Molecular Weight: 579.78
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: (Z)-2-(Benzhydrylidene-amino)-pent-2-enedioic acid 1-tert-butyl ester 5-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl] ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-(Benzhydrylidene-amino)-pent-2-enedioic acid 1-tert-butyl ester 5-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl] ester(342376-59-4)
EPA Substance Registry System: (Z)-2-(Benzhydrylidene-amino)-pent-2-enedioic acid 1-tert-butyl ester 5-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl] ester(342376-59-4)

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: 342376-59-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 342376-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,3,7 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 342376-59:
(8*3)+(7*4)+(6*2)+(5*3)+(4*7)+(3*6)+(2*5)+(1*9)=144
144 % 10 = 4
So 342376-59-4 is a valid CAS Registry Number.

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342376-59-4Relevant academic research and scientific papers

Conformationally restricted glutamic acid derivatives: Asymmetric synthesis of 4-substituted 4,5-dihydro-3(2H)-pyridazinones

Alvarez-Ibarra, Carlos,Csák?, Aurelio G.,Gómez de la Oliva, Cristina,Rodríguez, Eliazar

, p. 2129 - 2131 (2007/10/03)

The synthesis of optically pure 4,5-dihydro-3(2H)-pyridazinones substituted at C-4, which can be considered conformationally restricted cyclic Glu derivatives, has been accomplished by the asymmetric γ-alkylation of α,β-unsaturated glutamyl sultams under PTC conditions followed by reaction with hydrazines.

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