Cas 1114400-71-3,(S,E)-2-dibenzylamino-4-(2-pentadec-1-enyl-[1,3]-dioxolan-2-yl)-butanoic acid benzyl ester

1114400-71-3

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Basic information

Product Name: (S,E)-2-dibenzylamino-4-(2-pentadec-1-enyl-[1,3]-dioxolan-2-yl)-butanoic acid benzyl ester
Synonyms: (S,E)-2-dibenzylamino-4-(2-pentadec-1-enyl-[1,3]-dioxolan-2-yl)-butanoic acid benzyl ester
CAS NO:1114400-71-3
Molecular Formula:
Molecular Weight: 653.946
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: (S,E)-2-dibenzylamino-4-(2-pentadec-1-enyl-[1,3]-dioxolan-2-yl)-butanoic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S,E)-2-dibenzylamino-4-(2-pentadec-1-enyl-[1,3]-dioxolan-2-yl)-butanoic acid benzyl ester(1114400-71-3)
EPA Substance Registry System: (S,E)-2-dibenzylamino-4-(2-pentadec-1-enyl-[1,3]-dioxolan-2-yl)-butanoic acid benzyl ester(1114400-71-3)

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: 1114400-71-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1114400-71-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,4,4,0 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1114400-71:
(9*1)+(8*1)+(7*1)+(6*4)+(5*4)+(4*0)+(3*0)+(2*7)+(1*1)=83
83 % 10 = 3
So 1114400-71-3 is a valid CAS Registry Number.

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1114400-71-3Relevant academic research and scientific papers

Synthesis and application in SPPS of a stable amino acid isostere of palmitoyl cysteine

Cini, Elena,Lampariello, Lucia Raffaella,Rodriquez, Manuela,Taddei, Maurizio

experimental part, p. 844 - 848 (2009/04/07)

(S)-2-Amino-4-(2-pentadecyl-1,3-dioxolan-2-yl)-butanoic acid, 11, Pdiob, a synthetic analogue C-isostere of palmitoylated cysteine, has been prepared starting from tetrabenzyl glutamic acid. The less hindered benzyl carboxylate ester was transformed into

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