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41613-59-6

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41613-59-6 Usage

General Description

1-Ethynyl-2,2,6-trimethylcyclohexanol is a chemical compound that is commercially available in both the E and Z isomers at a purity of 97%. It contains a triple bond (ethynyl) and three methyl groups on a cyclohexane ring, giving it a unique structure and a high degree of stereochemical complexity. 1-Ethynyl-2,2,6-trimethylcyclohexanol, (E)+(Z), 97% has potential applications in organic synthesis, pharmaceuticals, and materials science due to its unique properties and reactivity. The high purity of the commercial product makes it suitable for a wide range of research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 41613-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,1 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41613-59:
(7*4)+(6*1)+(5*6)+(4*1)+(3*3)+(2*5)+(1*9)=96
96 % 10 = 6
So 41613-59-6 is a valid CAS Registry Number.

41613-59-6 Well-known Company Product Price

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  • Alfa Aesar

  • (B21057)  1-Ethynyl-2,2,6-trimethylcyclohexanol, (E)+(Z), 97%   

  • 41613-59-6

  • 5g

  • 663.0CNY

  • Detail
  • Alfa Aesar

  • (B21057)  1-Ethynyl-2,2,6-trimethylcyclohexanol, (E)+(Z), 97%   

  • 41613-59-6

  • 25g

  • 2659.0CNY

  • Detail

41613-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Ethynyl-2,2,6-trimethylcyclohexanol, (E)+(Z), 97%

1.2 Other means of identification

Product number -
Other names 1-ethynyl-2,2,6-trimethyl-1-cyclohexanol

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:41613-59-6 SDS

41613-59-6Relevant articles and documents

Synthesis of chlorins and bacteriochlorins from cycloaddition reactions with porphyrins

Cavaleiro, José A. S.,Monteiro, Carlos J. P.,Moura, Nuno M. M.,P. M. S. Neves, M. Gra?a,Tomé, Augusto C.

, (2022/02/10)

Chlorins and bacteriochlorins are reduced porphyrin-type derivatives displaying characteristic structural, physical, and chemical features. Such features make chlorins and bacteriochlorins key “players” in several fields, and specifically in medicine as p

USE OF SUBSTITUTED 1-(ARYL ETHYNYL)-, 1-(HETEROARYL ETHYNYL)-, 1-(HETEROCYCLYL ETHYNYL)- AND 1-(CYCLOALKENYL ETHYNYL)-CYCLOHEXANOLS AS ACTIVE AGENTS AGAINST ABIOTIC PLANT STRESS

-

Paragraph 0269, (2015/11/16)

The invention relates to the use of substituted 1-(arylethynyl)-, 1-(heteroarylethynyl)-, 1-(heterocyclylethynyl)- and 1-(cycloalkenylethynyl)cyclohexanols or salts thereof where the radicals in the general formula (I) correspond to the definitions given

98. A Regioselective Cyclohexannulation Procedure via Dienamine Cycloaddition. Synthesis of Functionalised Decalins

Snowden, Roger L.,Linder, Simon M.,Wuest, Manfred

, p. 892 - 905 (2007/10/02)

A regioselective cyclohexannulation procedure, whose key step involves the cycloaddition of dienamines 12-24 with methyl acrylate, allows the conversion of cycloalkanones 1-11 to bicyclic dienoates 25-37.The chemistry of 26 is briefly examined and, in the context of organoleptic studies concerning functionalised 5,5,9-trimethyldecalins, the transformation of 37 to ketones 44 and 46 as well as to acetates 53-56 is described.

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