Cas 873438-45-0,tert-Butyl-diphenyl-[(1R,2R,4S,5R)-5-((S)-toluene-4-sulfinyl)-4-vinyl-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethoxy]-silane

873438-45-0

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Basic information

Product Name: tert-Butyl-diphenyl-[(1R,2R,4S,5R)-5-((S)-toluene-4-sulfinyl)-4-vinyl-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethoxy]-silane
Synonyms: tert-Butyl-diphenyl-[(1R,2R,4S,5R)-5-((S)-toluene-4-sulfinyl)-4-vinyl-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethoxy]-silane
CAS NO:873438-45-0
Molecular Formula:
Molecular Weight: 518.749
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-diphenyl-[(1R,2R,4S,5R)-5-((S)-toluene-4-sulfinyl)-4-vinyl-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethoxy]-silane(CAS DataBase Reference)
NIST Chemistry Reference: tert-Butyl-diphenyl-[(1R,2R,4S,5R)-5-((S)-toluene-4-sulfinyl)-4-vinyl-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethoxy]-silane(873438-45-0)
EPA Substance Registry System: tert-Butyl-diphenyl-[(1R,2R,4S,5R)-5-((S)-toluene-4-sulfinyl)-4-vinyl-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethoxy]-silane(873438-45-0)

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: 873438-45-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 873438-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,4,3 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 873438-45:
(8*8)+(7*7)+(6*3)+(5*4)+(4*3)+(3*8)+(2*4)+(1*5)=200
200 % 10 = 0
So 873438-45-0 is a valid CAS Registry Number.

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873438-45-0Relevant academic research and scientific papers

Reductive cleavage of tetrahydrofuryl sulfur-substituted oxiranes: Application to the formal synthesis of Kumausyne and Kumausallene

Fernandez De La Pradilla, Roberto,Alhambra, Carolina,Castellanos, Alejandro,Fernandez, Jorge,Manzano, Pilar,Montero, Carlos,Urena, Mercedes,Viso, Alma

, p. 10693 - 10700 (2007/10/03)

Readily available sulfnyl and sulfonyl tetrahydrofuran methanol derivatives have been transformed efficiently into a variety of substituted tetrahydrofuryl alcohols by treatment with (PhSe)2 in the presence of an excess of NaBH4. Alt

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