Cas 1384752-91-3,prop-2-yn-1-yl 2,3,6-tri-O-benzoyl 4-O-[2,3,4,6-tetra-O-benzyl β-D-glucopyranosyl]β-D-glucopyranoside

1384752-91-3

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Basic information

Product Name: prop-2-yn-1-yl 2,3,6-tri-O-benzoyl 4-O-[2,3,4,6-tetra-O-benzyl β-D-glucopyranosyl]β-D-glucopyranoside
Synonyms:
CAS NO:1384752-91-3
Molecular Formula:
Molecular Weight: 1053.17
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: prop-2-yn-1-yl 2,3,6-tri-O-benzoyl 4-O-[2,3,4,6-tetra-O-benzyl β-D-glucopyranosyl]β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: prop-2-yn-1-yl 2,3,6-tri-O-benzoyl 4-O-[2,3,4,6-tetra-O-benzyl β-D-glucopyranosyl]β-D-glucopyranoside(1384752-91-3)
EPA Substance Registry System: prop-2-yn-1-yl 2,3,6-tri-O-benzoyl 4-O-[2,3,4,6-tetra-O-benzyl β-D-glucopyranosyl]β-D-glucopyranoside(1384752-91-3)

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: 1384752-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1384752-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,7,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1384752-91:
(9*1)+(8*3)+(7*8)+(6*4)+(5*7)+(4*5)+(3*2)+(2*9)+(1*1)=193
193 % 10 = 3
So 1384752-91-3 is a valid CAS Registry Number.

1384752-91-3Upstream product

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1384752-91-3Relevant academic research and scientific papers

Versatile gold catalyzed transglycosidation at ambient temperature

Kayastha, Abhijeet K.,Hotha, Srinivas

experimental part, p. 7161 - 7163 (2012/07/31)

Glycosidation with stable alkyl glycosyl donors using a catalytic amount of gold salts is promising. Herein, 1-ethynylcyclohexanyl glycosides are identified as novel donors at room temperature and mechanistic investigation showed that the leaving group simply extrudes out.

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