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Cyclohexene, 4-methoxy-1-methyl-4-(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94281-60-4

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94281-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94281-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,8 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 94281-60:
(7*9)+(6*4)+(5*2)+(4*8)+(3*1)+(2*6)+(1*0)=144
144 % 10 = 4
So 94281-60-4 is a valid CAS Registry Number.

94281-60-4SDS

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 4-methoxy-1-methyl-4-propan-2-ylcyclohexene

1.2 Other means of identification

Product number -
Other names Cyclohexene,4-methoxy-1-methyl-4-(1-methylethyl)

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:94281-60-4 SDS

94281-60-4Relevant academic research and scientific papers

Bis(phosphine)cobalt dialkyl complexes for directed catalytic alkene hydrogenation

Friedfeld, Max R.,Margulieux, Grant W.,Schaefer, Brian A.,Chirik, Paul J.

supporting information, p. 13178 - 13181 (2015/03/30)

Planar, low-spin cobalt(II) dialkyl complexes bearing bidentate phosphine ligands, (P - P)Co-(CH2SiMe3)2, are active for the hydrogenation of geminal and 1,2-disubstituted alkenes. Hydrogenation of more hindered internal and endocyclic trisubstituted alkenes was achieved through hydroxyl group activation, an approach that also enables directed hydrogenations to yield contrasteric isomers of cyclic alkanes.

Hydroalkoxylation of non-activated olefins catalysed by Lewis superacids in alcoholic solvents: an eco-friendly reaction

Lemechko, Pierre,Grau, Fanny,Antoniotti, Sylvain,Du?ach, Elisabet

, p. 5731 - 5734 (2008/02/09)

Lewis superacids such as tin(IV) triflate catalyse the intermolecular addition of primary alcohols to non-activated olefins under mild conditions.

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