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1H-Imidazole, 1-[[2-(4-pentynyl)cyclohexyl]thioxomethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88854-27-7

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88854-27-7 Usage

Imidazole Derivative

The compound is a derivative of imidazole, which is a five-membered ring with two non-adjacent nitrogen atoms.

Thioxomethyl Group

The compound contains a thioxomethyl group, which is a functional group derived from a thioaldehyde.

Pentynylcyclohexyl Group

The compound has a pentynylcyclohexyl group, which is a compound made up of a pentynyl group attached to a cyclohexyl ring.

Attachment to Imidazole Ring

The thioxomethyl group and the pentynylcyclohexyl group are both attached to the imidazole ring.

Potential Applications

This chemical may have applications in various fields such as pharmaceuticals, organic synthesis, or materials science.

Further Research

Further research may be needed to determine the specific uses and properties of 1H-Imidazole, 1-[[2-(4-pentynyl)cyclohexyl]thioxomethyl]-.

Check Digit Verification of cas no

The CAS Registry Mumber 88854-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,5 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88854-27:
(7*8)+(6*8)+(5*8)+(4*5)+(3*4)+(2*2)+(1*7)=187
187 % 10 = 7
So 88854-27-7 is a valid CAS Registry Number.

88854-27-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name imidazol-1-yl-(2-pent-4-ynylcyclohexyl)methanethione

1.2 Other means of identification

Product number -
Other names 1H-Imidazole,1-[[2-(4-pentynyl)cyclohexyl]thioxomethyl]

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:88854-27-7 SDS

88854-27-7Downstream Products

88854-27-7Relevant academic research and scientific papers

Synthesis of Ketones by Cyclization of Cyano and Acetylenic Radicals: Use of δ-Hydroxy Nitriles and δ- or ε-Hydroxy Acetylenes

Clive, Derrick L. J.,Beaulieu, Pierre L.,Set, Lu

, p. 1313 - 1314 (2007/10/02)

The radical intermediates generated by deoxygenation of alcohols undergo intramolecular ring closure when suitably located triple bonds (CC or CN) are present; the reaction provides a new synthesis of bicyclic ketones from either monocyclic ketones or cyclic olefins.

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