Cas 1365993-67-4,(2R,4S,5S,E,E)-1-tert-butoxycarbonyl-2-(trideca-6,8-dienyl)-4-hydroxy-5-aminopiperidine

1365993-67-4

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Basic information

Product Name: (2R,4S,5S,E,E)-1-tert-butoxycarbonyl-2-(trideca-6,8-dienyl)-4-hydroxy-5-aminopiperidine
Synonyms:
CAS NO:1365993-67-4
Molecular Formula:
Molecular Weight: 394.598
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: (2R,4S,5S,E,E)-1-tert-butoxycarbonyl-2-(trideca-6,8-dienyl)-4-hydroxy-5-aminopiperidine(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4S,5S,E,E)-1-tert-butoxycarbonyl-2-(trideca-6,8-dienyl)-4-hydroxy-5-aminopiperidine(1365993-67-4)
EPA Substance Registry System: (2R,4S,5S,E,E)-1-tert-butoxycarbonyl-2-(trideca-6,8-dienyl)-4-hydroxy-5-aminopiperidine(1365993-67-4)

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: 1365993-67-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1365993-67-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,9,9 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1365993-67:
(9*1)+(8*3)+(7*6)+(6*5)+(5*9)+(4*9)+(3*3)+(2*6)+(1*7)=214
214 % 10 = 4
So 1365993-67-4 is a valid CAS Registry Number.

1365993-67-4Upstream product

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1365993-67-4Relevant academic research and scientific papers

Polysubstituted piperidines via iodolactonization: Application to the asymmetric synthesis of (+)-pseudodistomin D

Davies, Stephen G.,Fletcher, Ai M.,Lee, James A.,Roberts, Paul M.,Russell, Angela J.,Taylor, Rachael J.,Thomson, Anthony D.,Thomson, James E.

, p. 1672 - 1675 (2012)

Conjugate addition of lithium (S)-N-allyl-N-(α-methyl-p- methoxybenzyl)amide to methyl (E,E)-hepta-2,5-dienoate furnished the corresponding β-amino ester. N-Protecting group manipulation, ring-closing metathesis, and ester hydrolysis gave enantiopure [N(1

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