Cas 119824-61-2,4-((2S,3R,4S,5R,6R)-3,4,5-Triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylsulfanyl)-butyric acid benzyl ester

119824-61-2

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Basic information

Product Name: 4-((2S,3R,4S,5R,6R)-3,4,5-Triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylsulfanyl)-butyric acid benzyl ester
Synonyms: 4-((2S,3R,4S,5R,6R)-3,4,5-Triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylsulfanyl)-butyric acid benzyl ester
CAS NO:119824-61-2
Molecular Formula:
Molecular Weight: 540.588
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: 4-((2S,3R,4S,5R,6R)-3,4,5-Triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylsulfanyl)-butyric acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-((2S,3R,4S,5R,6R)-3,4,5-Triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylsulfanyl)-butyric acid benzyl ester(119824-61-2)
EPA Substance Registry System: 4-((2S,3R,4S,5R,6R)-3,4,5-Triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylsulfanyl)-butyric acid benzyl ester(119824-61-2)

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: 119824-61-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 119824-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,2 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 119824-61:
(8*1)+(7*1)+(6*9)+(5*8)+(4*2)+(3*4)+(2*6)+(1*1)=142
142 % 10 = 2
So 119824-61-2 is a valid CAS Registry Number.

119824-61-2Upstream product

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119824-61-2Relevant academic research and scientific papers

FREE-RADICAL ADDITION OF 1-THIOSUGARS TO ALKENES A NEW GENERAL APPROACH TO THE SYNTHESIS OF 1-THIOGLYCOSIDES

Lacombe, J. M.,Rakotomanomana, N.,Pavia, A. A.

, p. 4293 - 4296 (1988)

Addition of peracetylated 1-thiosugars to alkenes in the presence of azobis(isobutironitrile) (AIBN) as initiator constitutes an efficient route to alkyl 1-thioglycosides as well as to 1-thioglycosides bearing a reactive group on the aglycon.

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