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Cyclohexanol, 1-(2-octynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69754-61-6

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69754-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69754-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,5 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69754-61:
(7*6)+(6*9)+(5*7)+(4*5)+(3*4)+(2*6)+(1*1)=176
176 % 10 = 6
So 69754-61-6 is a valid CAS Registry Number.

69754-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-oct-2-ynylcyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names Cyclohexanol,1-(2-octynyl)

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:69754-61-6 SDS

69754-61-6Downstream Products

69754-61-6Relevant academic research and scientific papers

Stereo- and regioselective metal salt-catalyzed alkynylation of 1,2-epoxides

Chini,Crotti,Favero,Macchia

, p. 6617 - 6620 (2007/10/02)

A simple, efficient, stereoselective, and highly regioselective method for the synthesis of β-hydroxyacetylenes by the direct opening of 1,2-epoxides with lithium acetylides in anhydrous THF, in the presence of metal salts, is described. This new method a

Selective Propargylation of Carbonyl Compounds with Allenylstannane/Alkyllithium Mixed Reagents

Suzuki, Masaaki,Morita, Yasushi,Noyori, Ryoji

, p. 441 - 449 (2007/10/02)

1-Substituted allenyltrialkylstannanes readily undergo transmetalation with an alkyllithium to generate a tetraalkylstannane and an equilibrating mixture of the allenyl- and propargyllithium compounds.The organolithium derivatives react with a variety of aldehydes and ketones at low temperature to give, after aqueous workup, the regioisomeric acetylenic and allenic carbinols in high yields.The degree of the regioselection is highly sensitive to the steric and electronic properties of the carbonyl substrates.Excellent acetylene selectivities are obtainable by combination of the bulky reagents and substrates or by using acylsilanes as carbonyl components.The origin of the regioselectivity is discussed.

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