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Benzenemethanol, 3,5-dimethoxy-a-2-propenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

647860-07-9

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647860-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 647860-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,7,8,6 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 647860-07:
(8*6)+(7*4)+(6*7)+(5*8)+(4*6)+(3*0)+(2*0)+(1*7)=189
189 % 10 = 9
So 647860-07-9 is a valid CAS Registry Number.

647860-07-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3',5'-dimethoxyphenyl)but-3-en-1-ol

1.2 Other means of identification

Product number -
Other names 1-(3,5-dimethoxyphenyl)but-3-en-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:647860-07-9 SDS

647860-07-9Relevant academic research and scientific papers

Remarkable Influence of Cobalt Catalysis on Epoxide Ring-Opening with Sulfoxonium Ylides

Jamieson, Megan L.,Brant, Nicola Z.,Brimble, Margaret A.,Furkert, Daniel P.

, p. 3952 - 3956 (2017/08/29)

Cobalt demonstrates a remarkable ability to catalytically divert the course of epoxide to oxetane ring expansion via reaction with a sulfoxonium ylide. An expanded survey of transition-metal catalysts has confirmed that cobalt salts uniquely instead deliv

One-pot sequential deoximation and allylation reactions of aldoximes in aqueous solution

Lin, Mei-Huey,Lin, Long-Zhi,Chuang, Tsung-Hsun,Liu, Han-Jun

experimental part, p. 2630 - 2635 (2012/04/23)

A simple procedure has been developed for conducting tin-mediated deoximation and allylation reactions of aldoximes in water to form homoallylic alcohols. Employing the new conditions, various homoallylic alcohols were produced in good to excellent yields

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