Cas 312300-77-9,1,2-di-O-octadecyl-3-O-(2,3,4-tri-O-acetyl-6-O-(p-toluenesulfonyl)-β-D-glucopyranosyl)glycerol

312300-77-9

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Basic information

Product Name: 1,2-di-O-octadecyl-3-O-(2,3,4-tri-O-acetyl-6-O-(p-toluenesulfonyl)-β-D-glucopyranosyl)glycerol
Synonyms: 1,2-di-O-octadecyl-3-O-(2,3,4-tri-O-acetyl-6-O-(p-toluenesulfonyl)-β-D-glucopyranosyl)glycerol
CAS NO:312300-77-9
Molecular Formula:
Molecular Weight: 1039.51
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: 1,2-di-O-octadecyl-3-O-(2,3,4-tri-O-acetyl-6-O-(p-toluenesulfonyl)-β-D-glucopyranosyl)glycerol(CAS DataBase Reference)
NIST Chemistry Reference: 1,2-di-O-octadecyl-3-O-(2,3,4-tri-O-acetyl-6-O-(p-toluenesulfonyl)-β-D-glucopyranosyl)glycerol(312300-77-9)
EPA Substance Registry System: 1,2-di-O-octadecyl-3-O-(2,3,4-tri-O-acetyl-6-O-(p-toluenesulfonyl)-β-D-glucopyranosyl)glycerol(312300-77-9)

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: 312300-77-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 312300-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,3,0 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 312300-77:
(8*3)+(7*1)+(6*2)+(5*3)+(4*0)+(3*0)+(2*7)+(1*7)=79
79 % 10 = 9
So 312300-77-9 is a valid CAS Registry Number.

312300-77-9Upstream product

312300-77-9Downstream Products

312300-77-9Relevant academic research and scientific papers

The synthesis of cationic glucosyl diglycerides

Alshoaibi,Morozova,Serebrennikova

, p. 633 - 636 (2007/10/03)

A series of glucosyl dialkylglycerols with the pyridinium, N-morpholinium, and N-methylimidazolium polar heads were synthesized by quaternization of the corresponding bases with the acetylated glucosyl diglyceride 6-O-methane- and 6-O-toluenesulfonates. The resulting compounds were designed for the use in gene delivery systems.

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