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1-ethynyl-3,3,5-trimethylcyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70487-02-4

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70487-02-4 Usage

Type of compound

Cyclohexanol derivative

Structural features

Ethynyl group (C≡CH) attached
Three methyl groups (CH3) attached to the cyclohexane ring

Common uses

Synthesis of pharmaceuticals and organic compounds
Potential medicinal properties (antifungal and antibacterial agent)
Production of fragrances and flavors

Industry applications

Pharmaceutical, chemical, and agricultural industries

Reactivity

Unique chemical structure and reactivity due to its functional groups and substitution pattern

Check Digit Verification of cas no

The CAS Registry Mumber 70487-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,8 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70487-02:
(7*7)+(6*0)+(5*4)+(4*8)+(3*7)+(2*0)+(1*2)=124
124 % 10 = 4
So 70487-02-4 is a valid CAS Registry Number.

70487-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethynyl-3,3,5-trimethylcyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names Opt.-inakt. 5-Hydroxy-1.1.3-trimethyl-5-aethinyl-cyclohexan

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:70487-02-4 SDS

70487-02-4Downstream Products

70487-02-4Relevant academic research and scientific papers

Unsaturated aldehydes as potential lilial replacers

Schroeder, Martin,Mathys, Marion,Ehrensperger, Nadja,Büchel, Michelle

, p. 1651 - 1673 (2015/02/19)

A series of Claisen rearrangements was undertaken in order to find a replacement for Lilial (= 3-(4-(tert-butyl)phenyl)-2-methylpropanal), a high-tonnage perfumery ingredient with a lily-of-the-valley odour, which is a CMR2 material [1]. 5,7,7-Trimethyl-4-methyleneoctanal (10), the synthesis of which is described, became the main lead. It possesses an odour which is very close to that of Lilial but lacks its substantivity. Aldehydes with higher molecular weights than that of 10 were, therefore, synthesised in order to boost substantivity and to understand the structural requirements for a 'Lilial' odour. The aldehydes were obtained via Claisen rearrangements of 'exo-methylidene' vinyl ethers, allenyl vinyl ethers, or allenyl allyl ethers. Alternatively, coupling of terminal alkynes with allyl alcohols led to the desired aldehydes. Derivatives of 10 and their sila analogues were also synthesised. The olfactory properties of all synthesised molecules were evaluated for possible structure-odour relationships (SOR).

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