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Benzene, [(1-butenyloxy)methyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89268-04-2

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89268-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89268-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,6 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89268-04:
(7*8)+(6*9)+(5*2)+(4*6)+(3*8)+(2*0)+(1*4)=172
172 % 10 = 2
So 89268-04-2 is a valid CAS Registry Number.

89268-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl (E)-1-butenyl ether

1.2 Other means of identification

Product number -
Other names [((E)-But-1-enyl)oxymethyl]-benzene

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:89268-04-2 SDS

89268-04-2Downstream Products

89268-04-2Relevant academic research and scientific papers

Visible-Light Controlled Divergent Catalysis Using a Bench-Stable Cobalt(I) Hydride Complex

Beltran, Frédéric,Bergamaschi, Enrico,Teskey, Christopher J.

supporting information, p. 5180 - 5184 (2020/04/22)

While the use of visible light in conjunction with transition metal catalysis offers powerful opportunities to switch between on/-off states of catalytic activity, the next frontier would be the ability to switch the actual function of the catalyst and resulting products. Here we report such an example of multi-dimensional catalysis. Featuring an easily prepared, bench-stable cobalt(I) hydride complex in conjunction with pinacolborane, we can switch the reaction outcome between two widely employed transformations, olefin migration and hydroboration, with visible light as the trigger.

Encapsulated molecular catalysts in polysiloxane gels: Ruthenium cluster-catalyzed isomerization of alkenes

Motoyama, Yukihiro,Abe, Motonori,Kamo, Kazuyuki,Kosako, Yusuke,Nagashima, Hideo

supporting information; experimental part, p. 5321 - 5323 (2009/03/11)

Novel ruthenium-encapsulating polysiloxane gels are prepared by treatment of polymethylhydrosiloxane with diols in the presence of (μ3, η2,η3,η5-acenaphthylene)Ru 3(CO)7, and act as reusable catalysts in the isomerization of alkenes without leakage of the catalyst species. The Royal Society of Chemistry.

A Convenient One-pot Synthesis of Polyenic Enol Ethers

Vo-Quang, Yen,Carniato, Denis,Vo-Quang Liliane,Goffic, Francois Le

, p. 1505 - 1506 (2007/10/02)

Diethyl alkoxymethylphosphonates react with unsaturated aldehydes to give polyenic enol ethers with a good stereoselectivity.

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