Cas 183901-68-0,(2S,3R,4E)-2',3',4',6'-tetra-O-benzoyl-β-D-glucopyranosyl-(1'->1)-2-(hexadecanoylamido)-3-O-benzoyl-4-octadecene-1,3-diol

183901-68-0

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Basic information

Product Name: (2S,3R,4E)-2',3',4',6'-tetra-O-benzoyl-β-D-glucopyranosyl-(1'->1)-2-(hexadecanoylamido)-3-O-benzoyl-4-octadecene-1,3-diol
Synonyms:
CAS NO:183901-68-0
Molecular Formula:
Molecular Weight: 1220.59
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: (2S,3R,4E)-2',3',4',6'-tetra-O-benzoyl-β-D-glucopyranosyl-(1'->1)-2-(hexadecanoylamido)-3-O-benzoyl-4-octadecene-1,3-diol(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R,4E)-2',3',4',6'-tetra-O-benzoyl-β-D-glucopyranosyl-(1'->1)-2-(hexadecanoylamido)-3-O-benzoyl-4-octadecene-1,3-diol(183901-68-0)
EPA Substance Registry System: (2S,3R,4E)-2',3',4',6'-tetra-O-benzoyl-β-D-glucopyranosyl-(1'->1)-2-(hexadecanoylamido)-3-O-benzoyl-4-octadecene-1,3-diol(183901-68-0)

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: 183901-68-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183901-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,9,0 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 183901-68:
(8*1)+(7*8)+(6*3)+(5*9)+(4*0)+(3*1)+(2*6)+(1*8)=150
150 % 10 = 0
So 183901-68-0 is a valid CAS Registry Number.

183901-68-0Upstream product

183901-68-0Downstream Products

74365-77-8 glucosylceramide

183901-68-0Relevant academic research and scientific papers

Efficient syntheses of a series of glycosphingolipids with 1,2-trans-glycosidic linkages

Liu, Yunpeng,Ding, Ning,Xiao, Hualing,Li, Yingxia

, p. 471 - 489 (2007/10/03)

A series of glycosphingolipids with 1,2-trans-glycosidic linkages were synthesized in the presence of neighboring group participation using trichloroacetimidates as glycosyl donors and an azido-sphingosine as the glycosyl acceptor. During the preparation

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