Cas 884382-60-9,(2R,3R,1'R,S<sub>S</sub>)-(E)-3-[1'-(tert-butyldimethylsilyloxy)-n-pentyl]-2-(1-pentenyl)-2-(p-tolylsulfinyl)oxirane

884382-60-9

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Basic information

Product Name: (2R,3R,1'R,S_S)-(E)-3-[1'-(tert-butyldimethylsilyloxy)-n-pentyl]-2-(1-pentenyl)-2-(p-tolylsulfinyl)oxirane
Synonyms: (2R,3R,1'R,S_S)-(E)-3-[1'-(tert-butyldimethylsilyloxy)-n-pentyl]-2-(1-pentenyl)-2-(p-tolylsulfinyl)oxirane
CAS NO:884382-60-9
Molecular Formula:
Molecular Weight: 450.758
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,1'R,S_S)-(E)-3-[1'-(tert-butyldimethylsilyloxy)-n-pentyl]-2-(1-pentenyl)-2-(p-tolylsulfinyl)oxirane(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,1'R,S_S)-(E)-3-[1'-(tert-butyldimethylsilyloxy)-n-pentyl]-2-(1-pentenyl)-2-(p-tolylsulfinyl)oxirane(884382-60-9)
EPA Substance Registry System: (2R,3R,1'R,S_S)-(E)-3-[1'-(tert-butyldimethylsilyloxy)-n-pentyl]-2-(1-pentenyl)-2-(p-tolylsulfinyl)oxirane(884382-60-9)

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: 884382-60-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 884382-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,3,8 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 884382-60:
(8*8)+(7*8)+(6*4)+(5*3)+(4*8)+(3*2)+(2*6)+(1*0)=209
209 % 10 = 9
So 884382-60-9 is a valid CAS Registry Number.

884382-60-9Upstream product

884382-60-9Downstream Products

884382-60-9Relevant academic research and scientific papers

Nucleophilic epoxidation of γ-alkoxy dienyl sulfoxide derivatives

Fernández De La Pradilla, Roberto,Victoria Buergo, María,Montero, Carlos,Viso, Alma

, p. 2684 - 2692 (2007/10/03)

(E,E) and (Z,E) γ-alkoxy dienyl sulfones undergo nucleophilic epoxidation with remarkable regio- and stereoselectivity to render syn oxiranes in a process mainly controlled by the alkoxy stereocenter. Upon epoxidation γ-hydroxy dienyl sulfoxides provide s

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