Cas 1542895-37-3,dibenzyl 1-((4S,6R,E)-6-((tert-butyldimethylsilyl)oxy)-1-ethoxy-1-oxonon-2-en-4-yl)hydrazine-1,2-dicarboxylate

1542895-37-3

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Basic information

Product Name: dibenzyl 1-((4S,6R,E)-6-((tert-butyldimethylsilyl)oxy)-1-ethoxy-1-oxonon-2-en-4-yl)hydrazine-1,2-dicarboxylate
Synonyms:
CAS NO:1542895-37-3
Molecular Formula:
Molecular Weight: 612.839
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: dibenzyl 1-((4S,6R,E)-6-((tert-butyldimethylsilyl)oxy)-1-ethoxy-1-oxonon-2-en-4-yl)hydrazine-1,2-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dibenzyl 1-((4S,6R,E)-6-((tert-butyldimethylsilyl)oxy)-1-ethoxy-1-oxonon-2-en-4-yl)hydrazine-1,2-dicarboxylate(1542895-37-3)
EPA Substance Registry System: dibenzyl 1-((4S,6R,E)-6-((tert-butyldimethylsilyl)oxy)-1-ethoxy-1-oxonon-2-en-4-yl)hydrazine-1,2-dicarboxylate(1542895-37-3)

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: 1542895-37-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1542895-37-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,2,8,9 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1542895-37:
(9*1)+(8*5)+(7*4)+(6*2)+(5*8)+(4*9)+(3*5)+(2*3)+(1*7)=193
193 % 10 = 3
So 1542895-37-3 is a valid CAS Registry Number.

1542895-37-3Upstream product

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1542895-37-3Relevant academic research and scientific papers

Organocatalytic stereoselective approach to the total synthesis of (-)-halosaline

Jha, Vishwajeet,Kumar, Pradeep

, p. 3238 - 3244 (2014)

A practical and efficient organocatalytic approach to the synthesis of substituted piperidine alkaloids in high enantio- and diastereomeric excess was achieved using proline-catalyzed sequential α-aminoxylation/α- amination reaction and HWE olefination reaction of an aldehyde.

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