Cas 117176-93-9,1,5-Anhydro-3-O-(tert-butyldiphenylsilyl)-2,6-didesoxy-L-arabino-hex-1-enitol

117176-93-9

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Basic information

Product Name: 1,5-Anhydro-3-O-(tert-butyldiphenylsilyl)-2,6-didesoxy-L-arabino-hex-1-enitol
Synonyms: 1,5-Anhydro-3-O-(tert-butyldiphenylsilyl)-2,6-didesoxy-L-arabino-hex-1-enitol
CAS NO:117176-93-9
Molecular Formula:
Molecular Weight: 368.548
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: 1,5-Anhydro-3-O-(tert-butyldiphenylsilyl)-2,6-didesoxy-L-arabino-hex-1-enitol(CAS DataBase Reference)
NIST Chemistry Reference: 1,5-Anhydro-3-O-(tert-butyldiphenylsilyl)-2,6-didesoxy-L-arabino-hex-1-enitol(117176-93-9)
EPA Substance Registry System: 1,5-Anhydro-3-O-(tert-butyldiphenylsilyl)-2,6-didesoxy-L-arabino-hex-1-enitol(117176-93-9)

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: 117176-93-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 117176-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,7 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117176-93:
(8*1)+(7*1)+(6*7)+(5*1)+(4*7)+(3*6)+(2*9)+(1*3)=129
129 % 10 = 9
So 117176-93-9 is a valid CAS Registry Number.

117176-93-9Upstream product

117176-93-9Downstream Products

117176-96-2 Benzyl-3-O-(tert-butyldiphenylsilyl)-2,6-didesoxy-2-iod-α-L-mannopyranosid

117176-93-9Relevant academic research and scientific papers

SELECTIVER AUFBAU α-L-(1->4)-VERKNUEPFTER 2,6-DIDESOXY-OLIGOSACCHARIDE

Thiem, Joachim,Klaffke, Werner,Springer, Dirk

, p. 201 - 210 (1988)

The phase-transfer catalyzed benzylation of 1,5-anhydro-2,6-dideoxy-L-arabino-hex-1-enitol (L-rhamnal, 5) led to a mixture of 4- and 3-O-benzyl derivatives in the ratio of 2:1.By silylation, 5 was regiospecifically transformed into either the 3-O-tert-but

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