Cas 108380-64-9,((E)-3-Bicyclo[2.2.1]hepta-2,5-dien-7-yl-1-[1,3]dioxolan-2-ylmethyl-allyloxy)-tert-butyl-dimethyl-silane

108380-64-9

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Basic information

Product Name: ((E)-3-Bicyclo[2.2.1]hepta-2,5-dien-7-yl-1-[1,3]dioxolan-2-ylmethyl-allyloxy)-tert-butyl-dimethyl-silane
Synonyms: ((E)-3-Bicyclo[2.2.1]hepta-2,5-dien-7-yl-1-[1,3]dioxolan-2-ylmethyl-allyloxy)-tert-butyl-dimethyl-silane
CAS NO:108380-64-9
Molecular Formula:
Molecular Weight: 348.558
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: ((E)-3-Bicyclo[2.2.1]hepta-2,5-dien-7-yl-1-[1,3]dioxolan-2-ylmethyl-allyloxy)-tert-butyl-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: ((E)-3-Bicyclo[2.2.1]hepta-2,5-dien-7-yl-1-[1,3]dioxolan-2-ylmethyl-allyloxy)-tert-butyl-dimethyl-silane(108380-64-9)
EPA Substance Registry System: ((E)-3-Bicyclo[2.2.1]hepta-2,5-dien-7-yl-1-[1,3]dioxolan-2-ylmethyl-allyloxy)-tert-butyl-dimethyl-silane(108380-64-9)

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: 108380-64-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 108380-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,8 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108380-64:
(8*1)+(7*0)+(6*8)+(5*3)+(4*8)+(3*0)+(2*6)+(1*4)=119
119 % 10 = 9
So 108380-64-9 is a valid CAS Registry Number.

108380-64-9Upstream product

5465-08-7 2-(β-Hydroxyethyl)-1,3-dioxolane

108380-64-9Downstream Products

108380-64-9Relevant academic research and scientific papers

Synthesis and Use of 7-Substituted Norbornadienes for the Preparation of Prostaglandins and Prostanoids

Baxter, Anthony D.,Binns, Falmai,Javed, Tariq,Roberts, Stanley M.,Sadler, Peter,et al.

, p. 889 - 900 (1986)

Syntheses of 7-substituted norbornadienes from 7-t-butoxy- and 7-halogeno-norbornadienes are described.Rearrangement of the products in the presence of peracetic acid gives bicyclic aldehydes (2) in equilibrium with enol ethers (3) which are hydrolysed to hydroxycyclopentenylacetaldehydes (4), and converted into key intermediates for the synthesis of prostaglandins and their analogues.Syntheses of prostaglandin J analogues with n-hexyl and phenyl groups replacing the ο-side-chain are described.

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