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26005-41-4

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26005-41-4 Usage

General Description

1-ETHYNYL-2,2,6-TRIMETHYLCYCLOHEXANOL is a synthetic chemical compound with the molecular formula C11H18O. It is a type of cycloalkanol with a triple bond attached to one of the carbon atoms. 1-ETHYNYL-2,2,6-TRIMETHYLCYCLOHEXANOL is used in various chemical reactions and processes, including as a building block in the synthesis of other organic compounds. It has potential applications in the pharmaceutical and agrochemical industries due to its unique structure and properties. However, as with any chemical, it is important to handle 1-ETHYNYL-2,2,6-TRIMETHYLCYCLOHEXANOL with caution and follow appropriate safety procedures to minimize any potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 26005-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,0 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26005-41:
(7*2)+(6*6)+(5*0)+(4*0)+(3*5)+(2*4)+(1*1)=74
74 % 10 = 4
So 26005-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O/c1-5-11(12)9(2)7-6-8-10(11,3)4/h1,9,12H,6-8H2,2-4H3/t9-,11+/m1/s1

26005-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ETHYNYL-2,2,6-TRIMETHYLCYCLOHEXANOL

1.2 Other means of identification

Product number -
Other names Z-1-Ethynyl-2,2,6-trimethyl-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:26005-41-4 SDS

26005-41-4Relevant articles and documents

The Diels-Alder Route to Drimane related Sesquiterpenes; Synthesis of Cinnamolide, Polygodial, Isodrimeninol, Drimenin and Warburganal

Hollinshead, David M.,Howell, S. Christopher,Ley, Steven V.,Mahon, Michael,Ratcliffe, Norman M.,Worthington, Paul A.

, p. 1579 - 1589 (2007/10/02)

The stereospecific preparation of various 1-vinyl-2,6,6-trimethylcyclohex-1-enes (6) as potential diene precursors in the Diels-Alder reaction with dimethyl acetylenedicarboxylate have been investigated.The reaction of the parent diene (6a) with dimethyl acetylenedicarboxylate affords an adduct (18) in 94percent yield.This species was reductively isomerised using 10percent Pd/C/H2 and a mineral acid to give a trans-fused decalin diester (19).Reduction of (19) with lithium aluminium hydride afforded 1,4,4a,5,6,8,8a-octahydro-5,8,8a-trimethyl-1β,4aα,8aβ-naphthalene-1,2-dimethanol (24) a key starting material for the highly efficient syntheses of five drimane sesquiterpene natural products, cinnamolide (1), polygodial (2), isodrimeninol (3), drimenin (4), and warbuganal (5).Microbial oxidation reactions using C. elegans or A. niger of (2), (24), and (1) gave good yields of the corresponding 3β-hydroxy derivatives, (30), (31), and (32).Several other unusually substituted drimane derivatives are reported.

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