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

24580-53-8

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24580-53-8 Usage

1-ethynyl-3-methylcyclohexanol Properties

2. Cyclohexanol derivative
3. Ethynyl group at the 1 position
4. Methyl group at the 3 position
5. Commonly used in organic synthesis
6. Building block for various organic compounds
7. Potential biological activities
8. Pharmacological properties
9. Used as a reagent in pharmaceutical and agrochemical synthesis
10. Versatile chemical reactivity
11. Functional group compatibility

Check Digit Verification of cas no

The CAS Registry Mumber 24580-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,8 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24580-53:
(7*2)+(6*4)+(5*5)+(4*8)+(3*0)+(2*5)+(1*3)=108
108 % 10 = 8
So 24580-53-8 is a valid CAS Registry Number.

24580-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethynyl-3-methylcyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Aethinyl-3-methyl-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:24580-53-8 SDS

24580-53-8Relevant academic research and scientific papers

Synthesis of acetylenic alcohols with calcium carbide as the acetylene source

Sum, Yin Ngai,Yu, Dingyi,Zhang, Yugen

supporting information, p. 2718 - 2721 (2013/10/08)

Propargyl alcohols containing a terminal alkyne group are highly important and versatile intermediates. Here, we report the synthesis of these compounds from an inexpensive and renewable resource, calcium carbide (CaC2). No metal catalysts are required in this new protocol and the reactions take place under very mild conditions.

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