Cas 206654-16-2,Benzoic acid (2R,3S,4S,5S)-5-bromo-3-(tert-butyl-dimethyl-silanyloxy)-2-methoxy-tetrahydro-pyran-4-yl ester

206654-16-2

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Basic information

Product Name: Benzoic acid (2R,3S,4S,5S)-5-bromo-3-(tert-butyl-dimethyl-silanyloxy)-2-methoxy-tetrahydro-pyran-4-yl ester
Synonyms: Benzoic acid (2R,3S,4S,5S)-5-bromo-3-(tert-butyl-dimethyl-silanyloxy)-2-methoxy-tetrahydro-pyran-4-yl ester
CAS NO:206654-16-2
Molecular Formula:
Molecular Weight: 445.426
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: Benzoic acid (2R,3S,4S,5S)-5-bromo-3-(tert-butyl-dimethyl-silanyloxy)-2-methoxy-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (2R,3S,4S,5S)-5-bromo-3-(tert-butyl-dimethyl-silanyloxy)-2-methoxy-tetrahydro-pyran-4-yl ester(206654-16-2)
EPA Substance Registry System: Benzoic acid (2R,3S,4S,5S)-5-bromo-3-(tert-butyl-dimethyl-silanyloxy)-2-methoxy-tetrahydro-pyran-4-yl ester(206654-16-2)

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: 206654-16-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 206654-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,6,5 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 206654-16:
(8*2)+(7*0)+(6*6)+(5*6)+(4*5)+(3*4)+(2*1)+(1*6)=122
122 % 10 = 2
So 206654-16-2 is a valid CAS Registry Number.

206654-16-2Upstream product

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206654-16-2Relevant academic research and scientific papers

Synthesis of Bridgehead-Functionalized Bicyclo[3.2.1]octanes via Intramolecular Titanium- and Tributylstannane-Induced Pinacol Coupling

Egger, Anita,Hunziker, Jurg,Rihs, Grethy,Leumann, Christian

, p. 734 - 743 (1998)

The synthesis of the enantiomerically pure, bridgehead-functionalized bicyclo[3.2.1]octanes 11 and 16, containing a conformationally fixed trihydroxypropyl (aminodihydroxypropyl) unit, as well as the X-ray structure of 11 are described. These compounds ar

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