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52718-65-7

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52718-65-7 Usage

General Description

1-methylcyclohexane-1,2-diol is a chemical compound with the molecular formula C7H14O2. It belongs to the class of alcohols and contains a cyclohexane ring with a methyl group and two hydroxyl groups attached. 1-methylcyclohexane-1,2-diol is known for its use as a building block in organic synthesis and as a solvent in various chemical reactions. It has also been studied for its potential pharmaceutical and biological applications. 1-methylcyclohexane-1,2-diol is considered to be a valuable intermediate in the production of various fine chemicals and can be found in various industrial and research settings.

Check Digit Verification of cas no

The CAS Registry Mumber 52718-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,1 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52718-65:
(7*5)+(6*2)+(5*7)+(4*1)+(3*8)+(2*6)+(1*5)=127
127 % 10 = 7
So 52718-65-7 is a valid CAS Registry Number.

52718-65-7SDS

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 trans-1-methylcyclohexane-1,2-diol

1.2 Other means of identification

Product number -
Other names 1-methyl-trans-cyclohexane-1,2-diol

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:52718-65-7 SDS

52718-65-7Relevant articles and documents

Selective Isomerization via Transient Thermodynamic Control: Dynamic Epimerization of trans to cis Diols

Macmillan, David W. C.,Oswood, Christian J.

, p. 93 - 98 (2022/01/03)

Traditional approaches to stereoselective synthesis require high levels of enantio- and diastereocontrol in every step that forms a new stereocenter. Here, we report an alternative approach, in which the stereochemistry of organic substrates is selectivel

Photo-Induced Dihydroxylation of Alkenes with Diacetyl, Oxygen, and Water

Masuda, Yusuke,Ikeshita, Daichi,Murakami, Masahiro

, (2021/02/09)

Herein reported is a photo-induced production of vicinal diols from alkenes under mild reaction conditions. The present dihydroxylation method using diacetyl (= butane-2,3-dione), oxygen, and water dispenses with toxic reagents and intractable waste generation.

Hydrodealkenylative C(sp3)–C(sp2) bond fragmentation

Smaligo, Andrew J.,Swain, Manisha,Quintana, Jason C.,Tan, Mikayla F.,Kim, Danielle A.,Kwon, Ohyun

, p. 681 - 685 (2019/06/11)

Chemical synthesis typically relies on reactions that generate complexity through elaboration of simple starting materials. Less common are deconstructive strategies toward complexity—particularly those involving carbon-carbon bond scission. Here, we introduce one such transformation: the hydrodealkenylative cleavage of C(sp3)–C(sp2) bonds, conducted below room temperature, using ozone, an iron salt, and a hydrogen atom donor. These reactions are performed in nonanhydrous solvents and open to the air; reach completion within 30 minutes; and deliver their products in high yields, even on decagram scales. We have used this broadly functionality tolerant transformation to produce desirable synthetic intermediates, many of which are optically active, from abundantly available terpenes and terpenoid-derived precursors. We have also applied it in the formal total syntheses of complex molecules.

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