Cas 473791-28-5,((2R,3R,4aS,5R,8aR)-7-Benzenesulfinylmethyl-2,3-dimethoxy-2,3-dimethyl-2,3,4a,5,8,8a-hexahydro-benzo[1,4]dioxin-5-yloxy)-tert-butyl-dimethyl-silane

473791-28-5

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Product Name: ((2R,3R,4aS,5R,8aR)-7-Benzenesulfinylmethyl-2,3-dimethoxy-2,3-dimethyl-2,3,4a,5,8,8a-hexahydro-benzo[1,4]dioxin-5-yloxy)-tert-butyl-dimethyl-silane
Synonyms: ((2R,3R,4aS,5R,8aR)-7-Benzenesulfinylmethyl-2,3-dimethoxy-2,3-dimethyl-2,3,4a,5,8,8a-hexahydro-benzo[1,4]dioxin-5-yloxy)-tert-butyl-dimethyl-silane
CAS NO:473791-28-5
Molecular Formula:
Molecular Weight: 496.74
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,3R,4aS,5R,8aR)-7-Benzenesulfinylmethyl-2,3-dimethoxy-2,3-dimethyl-2,3,4a,5,8,8a-hexahydro-benzo[1,4]dioxin-5-yloxy)-tert-butyl-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: ((2R,3R,4aS,5R,8aR)-7-Benzenesulfinylmethyl-2,3-dimethoxy-2,3-dimethyl-2,3,4a,5,8,8a-hexahydro-benzo[1,4]dioxin-5-yloxy)-tert-butyl-dimethyl-silane(473791-28-5)
EPA Substance Registry System: ((2R,3R,4aS,5R,8aR)-7-Benzenesulfinylmethyl-2,3-dimethoxy-2,3-dimethyl-2,3,4a,5,8,8a-hexahydro-benzo[1,4]dioxin-5-yloxy)-tert-butyl-dimethyl-silane(473791-28-5)

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: 473791-28-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 473791-28-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,7,9 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 473791-28:
(8*4)+(7*7)+(6*3)+(5*7)+(4*9)+(3*1)+(2*2)+(1*8)=185
185 % 10 = 5
So 473791-28-5 is a valid CAS Registry Number.

473791-28-5Upstream product

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473791-28-5Relevant academic research and scientific papers

Syntheses of gabosine A, B, D, and E from allyl sulfide derived from (-)-quinic acid

Shinada, Tetsuro,Fuji, Toshiyuki,Ohtani, Yasuhiro,Yoshida, Yasutaka,Ohfune, Yasufumi

, p. 1341 - 1343 (2002)

An efficient conversion of allyl sulfide 6 prepared from (-)-quinic acid (5) to gabosines was achieved by a series of sequential reactions: i) Mislow-Evans rearrangement, ii) SeO2 oxidation, iii) conjugate addition of sodium hydroxide or sodium

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