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Cyclohexanemethanol, a-[1-(trimethylsilyl)-1,2-propadienyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79015-68-2

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79015-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79015-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,1 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79015-68:
(7*7)+(6*9)+(5*0)+(4*1)+(3*5)+(2*6)+(1*8)=142
142 % 10 = 2
So 79015-68-2 is a valid CAS Registry Number.

79015-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-2-(trimethylsilyl)-2,3-butadien-1-ol

1.2 Other means of identification

Product number -
Other names 1-cyclohexyl-2-trimethylsilyl-2,3-butadien-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:79015-68-2 SDS

79015-68-2Relevant academic research and scientific papers

On pentaorganylstiborane. III. Regio- and diastereoselective additions of acetylenic and allenic organoantimony compounds to aldehydes

Zhang, Li-Jun,Mo, Xue-Sheng,Huang, Yao-Zeng

, p. 77 - 86 (2007/10/02)

The reaction of propargyl bromide (4a) with tributylstibine gave allenyltributylstibonium bromide (5), and its corresponding pentaorganylstiborane reacted with aldehyde to give homopropargylic alcohol (10a) exclusively in good yield.However, the reaction

Regioselective reactions of trimethylsilylpropargylic and trimethylsilylallylic organoantimony compounds with aldehydes

Zhang, Li-Jun,Mo, Xue-Sheng,Huang, Ji-Ling,Huang, Yao-Zeng

, p. 1621 - 1624 (2007/10/02)

The reactions of trimethylsilylallylic organoantimony compound with aldehydes show very high selectivity favoring α-adducts; and the reactions of trimethylsilylpropargylic organoantimony compounds with aldehydes also exhibit very high acetylenic selectivity (α-adducts) in the presence of LiBr.

Regio- and Stereocontrolled Synthesis of Allenic and Acetylenic Derivatives. Organotitanium and Boron Reagents

Furuta, Kyoji,Ishiguro, Masaharu,Haruta, Ryuichi,Ikeda, Nobuo,Yamamoto, Hisashi

, p. 2768 - 2776 (2007/10/02)

The propargyltitanium reagents derived from 1-alkylpropyne condensed with aldehydes to give α-allenyl alcohol regioselectively, while the allenyltitanium reagents generated from 1-alkyl-1-butyne derivatives gave threo-β-acetylenic alcohols with high regio- and stereoselectivities.The course of the reaction was determined by the substitution pattern of starting alkynes.The similar reactions of metallated 1,3-bis(trialkylsilyl)propyne or (trialkylsilyl)acetonitrile with aldehydes were also investigated.

Propargylic Titanium Reagents. Regio- and Stereocontrolled Synthesis of Allenic and Acetylenic Alcohols

Ishiguro, Masaharu,Yamamoto, Nobuo Ikeda Hisashi

, p. 2225 - 2227 (2007/10/02)

The highly selective condensations of propargylic titanium reagents and aldehydes are described.

SILANES IN ORGANIC SYNTHESIS. 11. REGIOCONTROLLED SYNTHESIS OF α-HYDROXYMETHYLATED (TRIMETHYLSILYL)ALLENES

Daniels, Rhys G.,Paquette, Leo A.

, p. 1579 - 1582 (2007/10/02)

The organometallic produced by reaction of trimethylsilylpropargyl bromide with aluminium amalgam in anhydrous tetrahydrofuran condenses readily with aldehydes and ketones to give allenic alcohols resulting from coupling α to the trimethylsilyl substituen

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