Cas 131968-54-2,(2R,3S,4R,5R,6S)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-6-phenyl-tetrahydro-pyran-4-ol

131968-54-2

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Basic information

Product Name: (2R,3S,4R,5R,6S)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-6-phenyl-tetrahydro-pyran-4-ol
Synonyms: (2R,3S,4R,5R,6S)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-6-phenyl-tetrahydro-pyran-4-ol
CAS NO:131968-54-2
Molecular Formula:
Molecular Weight: 583.044
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: (2R,3S,4R,5R,6S)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-6-phenyl-tetrahydro-pyran-4-ol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,4R,5R,6S)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-6-phenyl-tetrahydro-pyran-4-ol(131968-54-2)
EPA Substance Registry System: (2R,3S,4R,5R,6S)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-6-phenyl-tetrahydro-pyran-4-ol(131968-54-2)

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: 131968-54-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 131968-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,9,6 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131968-54:
(8*1)+(7*3)+(6*1)+(5*9)+(4*6)+(3*8)+(2*5)+(1*4)=142
142 % 10 = 2
So 131968-54-2 is a valid CAS Registry Number.

131968-54-2Upstream product

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131968-54-2Relevant academic research and scientific papers

Hydroboration of C-arylglucals. Synthesis of the β-C-arylglucoside nucleus of chaetiacandin

Friesen,Daljeet

, p. 6133 - 6136 (2007/10/02)

The hydroborations of the C-arylglucals 3a-c obtained from palladium catalyzed coupling reactions, provide the corresponding β-C-arylglucosides. Depending upon the conditions chosen for the oxidative workup, either the alcohols 5a-c or the products resulting from silyl migration (4a-c) are readily obtained. The palladium catalyzed coupling-hydroboration sequence has been applied to the synthesis of the β-C-arylglucoside nucleus of chaetiacandin, an anti-yeast antibiotic of the papulacandin family.

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