Cas 110224-84-5,Acetic acid (2R,3S,4S,5R)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((3aR,4R,6S,7S,7aR)-4-methoxy-2,2,6-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yloxy)-tetrahydro-pyran-4-yl ester

110224-84-5

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Basic information

Product Name: Acetic acid (2R,3S,4S,5R)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((3aR,4R,6S,7S,7aR)-4-methoxy-2,2,6-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yloxy)-tetrahydro-pyran-4-yl ester
Synonyms:
CAS NO:110224-84-5
Molecular Formula:
Molecular Weight: 692.804
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: Acetic acid (2R,3S,4S,5R)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((3aR,4R,6S,7S,7aR)-4-methoxy-2,2,6-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yloxy)-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3S,4S,5R)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((3aR,4R,6S,7S,7aR)-4-methoxy-2,2,6-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yloxy)-tetrahydro-pyran-4-yl ester(110224-84-5)
EPA Substance Registry System: Acetic acid (2R,3S,4S,5R)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((3aR,4R,6S,7S,7aR)-4-methoxy-2,2,6-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yloxy)-tetrahydro-pyran-4-yl ester(110224-84-5)

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: 110224-84-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110224-84-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,2 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 110224-84:
(8*1)+(7*1)+(6*0)+(5*2)+(4*2)+(3*4)+(2*8)+(1*4)=65
65 % 10 = 5
So 110224-84-5 is a valid CAS Registry Number.

110224-84-5Upstream product

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110224-84-5Relevant academic research and scientific papers

A New Method for The Synthesis of O-Glycosides from S-Glycosides

Pozsgay, Vince,Jennings, Harold J.

, p. 4635 - 4637 (1987)

Treatment of S-glycosides with NOBF4 produced highly reactive glycosyl donors which in the presence of glycosyl acceptors gave O-glycosides in high yields.

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