Cas 714966-82-2,(E)-3-{2-[(Z)-6-(tert-Butyl-dimethyl-silanyloxy)-hex-3-enyl]-4-methoxy-phenyl}-prop-2-en-1-ol

714966-82-2

Post Buying Request

Basic information

Product Name: (E)-3-{2-[(Z)-6-(tert-Butyl-dimethyl-silanyloxy)-hex-3-enyl]-4-methoxy-phenyl}-prop-2-en-1-ol
Synonyms:
CAS NO:714966-82-2
Molecular Formula:
Molecular Weight: 376.612
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-{2-[(Z)-6-(tert-Butyl-dimethyl-silanyloxy)-hex-3-enyl]-4-methoxy-phenyl}-prop-2-en-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-{2-[(Z)-6-(tert-Butyl-dimethyl-silanyloxy)-hex-3-enyl]-4-methoxy-phenyl}-prop-2-en-1-ol(714966-82-2)
EPA Substance Registry System: (E)-3-{2-[(Z)-6-(tert-Butyl-dimethyl-silanyloxy)-hex-3-enyl]-4-methoxy-phenyl}-prop-2-en-1-ol(714966-82-2)

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: 714966-82-2(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

714966-82-2 Suppliers

Recommended suppliers

714966-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 714966-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,4,9,6 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 714966-82:
(8*7)+(7*1)+(6*4)+(5*9)+(4*6)+(3*6)+(2*8)+(1*2)=192
192 % 10 = 2
So 714966-82-2 is a valid CAS Registry Number.

714966-82-2Upstream product

714966-82-2Downstream Products

714966-82-2Relevant academic research and scientific papers

A new total synthesis of (±)-oestrone

Pattenden, Gerald,Reddy, L. Krishnakanth,Walter, Affo

, p. 4027 - 4030 (2007/10/03)

A conceptually new total synthesis of oestrone, based on a novel cascade of radical cyclisations from the iodo aryl vinylcyclopropane 2, via 10, 15, 16 and 17, leading to the intermediate trans,anti,trans-oestradiol derivative 11 in one step, is described. Oxidation of 11, followed by demethylation of the resulting aryl methyl ether 18 then gives (±)-oestrone 1.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 714966-82-2