Cas 454472-14-1,15-(benzyloxy-carbonyloctadecyl-amino)-pentadecyl-β-D-2,3,4,6-tetra-O-acetylmanno-pyranoside

454472-14-1

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Basic information

Product Name: 15-(benzyloxy-carbonyloctadecyl-amino)-pentadecyl-β-D-2,3,4,6-tetra-O-acetylmanno-pyranoside
Synonyms: 15-(benzyloxy-carbonyloctadecyl-amino)-pentadecyl-β-D-2,3,4,6-tetra-O-acetylmanno-pyranoside
CAS NO:454472-14-1
Molecular Formula:
Molecular Weight: 960.343
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: 15-(benzyloxy-carbonyloctadecyl-amino)-pentadecyl-β-D-2,3,4,6-tetra-O-acetylmanno-pyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 15-(benzyloxy-carbonyloctadecyl-amino)-pentadecyl-β-D-2,3,4,6-tetra-O-acetylmanno-pyranoside(454472-14-1)
EPA Substance Registry System: 15-(benzyloxy-carbonyloctadecyl-amino)-pentadecyl-β-D-2,3,4,6-tetra-O-acetylmanno-pyranoside(454472-14-1)

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: 454472-14-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 454472-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,4,7 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 454472-14:
(8*4)+(7*5)+(6*4)+(5*4)+(4*7)+(3*2)+(2*1)+(1*4)=151
151 % 10 = 1
So 454472-14-1 is a valid CAS Registry Number.

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454472-14-1Relevant academic research and scientific papers

Glycosidation of alkylamino-alkan-1-ol. A simple and convenient synthesis of glycosylated cationic lipids.

Jacopin, Christophe,Egron, Marie-Jose,Scherman, Daniel,Herscovici, Jean

, p. 1447 - 1450 (2007/10/03)

Starting from long chain alkylamino-alkan-1-ol a series of amino glycolipids were synthesized. This procedure allows a short and convenient preparation of glycosylated cationic lipids for gene delivery.

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