Cas 1056759-77-3,tert-butyl(dimethyl){[(2S,3S,4S)-2,3,4-tri(benzyloxy)hex-5-en-1-yl]oxy}silane

1056759-77-3

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Basic information

Product Name: tert-butyl(dimethyl){[(2S,3S,4S)-2,3,4-tri(benzyloxy)hex-5-en-1-yl]oxy}silane
Synonyms: tert-butyl(dimethyl){[(2S,3S,4S)-2,3,4-tri(benzyloxy)hex-5-en-1-yl]oxy}silane
CAS NO:1056759-77-3
Molecular Formula:
Molecular Weight: 532.795
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: tert-butyl(dimethyl){[(2S,3S,4S)-2,3,4-tri(benzyloxy)hex-5-en-1-yl]oxy}silane(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl(dimethyl){[(2S,3S,4S)-2,3,4-tri(benzyloxy)hex-5-en-1-yl]oxy}silane(1056759-77-3)
EPA Substance Registry System: tert-butyl(dimethyl){[(2S,3S,4S)-2,3,4-tri(benzyloxy)hex-5-en-1-yl]oxy}silane(1056759-77-3)

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: 1056759-77-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1056759-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,6,7,5 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1056759-77:
(9*1)+(8*0)+(7*5)+(6*6)+(5*7)+(4*5)+(3*9)+(2*7)+(1*7)=183
183 % 10 = 3
So 1056759-77-3 is a valid CAS Registry Number.

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1056759-77-3Relevant academic research and scientific papers

An efficient synthesis of triazolo-carbohydrate mimetics and their conformational analysis

Yanai, Hikaru,Obara, Shun,Taguchi, Takeo

supporting information; experimental part, p. 2679 - 2685 (2009/02/03)

A chemical library of 1,2,3-triazole fused carbohydrate mimetics was constructed. To synthesize enantiomerically pure mimetics, we developed a stereo- or diastereodivergent synthetic route from d-glucose, d-mannose and d-galactose as chiral sources. In th

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