Cas 1379827-90-3,2-(S)-phenyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-β-D-glucopyranoso)[1,2-e]-1,4-oxathiane-S-oxide

1379827-90-3

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Basic information

Product Name: 2-(S)-phenyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-β-D-glucopyranoso)[1,2-e]-1,4-oxathiane-S-oxide
Synonyms: 2-(S)-phenyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-β-D-glucopyranoso)[1,2-e]-1,4-oxathiane-S-oxide
CAS NO:1379827-90-3
Molecular Formula:
Molecular Weight: 442.472
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: 2-(S)-phenyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-β-D-glucopyranoso)[1,2-e]-1,4-oxathiane-S-oxide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(S)-phenyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-β-D-glucopyranoso)[1,2-e]-1,4-oxathiane-S-oxide(1379827-90-3)
EPA Substance Registry System: 2-(S)-phenyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-β-D-glucopyranoso)[1,2-e]-1,4-oxathiane-S-oxide(1379827-90-3)

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: 1379827-90-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1379827-90-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,8,2 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1379827-90:
(9*1)+(8*3)+(7*7)+(6*9)+(5*8)+(4*2)+(3*7)+(2*9)+(1*0)=223
223 % 10 = 3
So 1379827-90-3 is a valid CAS Registry Number.

1379827-90-3Upstream product

1361996-85-1 2-(S)-phenyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-β-D-glucopyranoso)[1,2-e]-1,4-oxathiane (S)-S-oxide

1379827-90-3Downstream Products

1379827-90-3Relevant academic research and scientific papers

Mechanistic studies on a sulfoxide transfer reaction mediated by diphenyl sulfoxide/triflic anhydride

Fascione, Martin A.,Adshead, Sophie J.,Mandal, Pintu K.,Kilner, Colin A.,Leach, Andrew G.,Turnbull, W. Bruce

supporting information; experimental part, p. 2987 - 2997 (2012/04/23)

Sulfoxides are frequently used in organic synthesis as chiral auxiliaries and reagents to mediate a wide variety of chemical transformations. For example, diphenyl sulfoxide and triflic anhydride can be used to activate a wide range of glycosyl donors inc

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