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2-Propen-1-one, 1-cyclohexyl-3-(trimethylsilyl)-, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115505-23-2

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115505-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115505-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,5,0 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115505-23:
(8*1)+(7*1)+(6*5)+(5*5)+(4*0)+(3*5)+(2*2)+(1*3)=92
92 % 10 = 2
So 115505-23-2 is a valid CAS Registry Number.

115505-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-3-trimethylsilylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names -

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:115505-23-2 SDS

115505-23-2Downstream Products

115505-23-2Relevant academic research and scientific papers

Ruthenium-catalysed synthesis of functional conjugated dienes from propargylic carbonates and silyl diazo compounds

Moulin, Solenne,Zhang, Hanyu,Raju, Suresh,Bruneau, Christian,Dérien, Sylvie

, p. 3292 - 3296 (2013/07/19)

The reactions of propargylic carbonates with silyl diazo compounds in the presence of [Cp*RuClACHTUNGTRENUNG(cod)] as a catalyst precursor. Copyright

A convergent regiospecific synthesis of zirconium enolates

Kasatkin, Aleksandra,Whitby, Richard J.

, p. 9857 - 9864 (2007/10/03)

α-Lithiated phenylsulphonyloxiranes insert into alkenylzirconocene chlorides with loss of phenylsulphinate to give zirconyloxiranes which smoothly rearrange by either α- or β- C-O cleavage to afford regiodefined zirconium enolates which may be further elaborated.

Silyl Derivatives in the Synthesis of trans-β-Trimethylsilyl-α,β-unsaturated Ketones

Christiansen, Mette Lene,Benneche, Tore,Undheim, Kjell

, p. 536 - 540 (2007/10/02)

Methods for the preparation of α-halo-α-(trimethylsilyl)methyl ethers are described.These substances react with (trimethylsilyl)methyl ketones to yield β-methoxy-β-(trimethylsilyl)ethyl ketones.Sodium trimethylsilanoate in dichloromethane solution has bee

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