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6296-84-0

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6296-84-0 Usage

General Description

1-Methylcyclohexane-1,2-diol, also known as 1-methylcyclohexan-1,2-diol, is an organic compound with the chemical formula C7H14O2. It is a colorless, viscous liquid with a slightly sweet odor. This chemical is used primarily as a solvent in various industrial applications, including the production of coatings, paints, and adhesives. It is also used as a stabilizer in the formulation of pharmaceuticals and as a dispersant in the manufacture of pigments. Additionally, 1-methylcyclohexane-1,2-diol can act as a chiral building block in organic synthesis, making it a versatile compound with multiple uses in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 6296-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6296-84:
(6*6)+(5*2)+(4*9)+(3*6)+(2*8)+(1*4)=120
120 % 10 = 0
So 6296-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2/c1-7(9)5-3-2-4-6(7)8/h6,8-9H,2-5H2,1H3

6296-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylcyclohexane-1,2-diol

1.2 Other means of identification

Product number -
Other names trans-1-methylcyclohexane-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:6296-84-0 SDS

6296-84-0Relevant articles and documents

Oxidation of alkenes to 1,2-diols: FT-IR and UV studies of silica-supported sulfonic acid catalysts and their interaction with H2O and H 2O2

Maggi, Raimondo,Martra, Gianmario,Piscopo, Calogero Giancarlo,Alberto, Gabriele,Sartori, Giovanni

, p. 19 - 28 (2012)

Supported sulfonic acids can be employed as efficient catalysts in the dihydroxylation of 1-methylcyclohexene with aqueous hydrogen peroxide, without the use of additional solvents, under mild condition. The reaction was deeply studied in terms of catalys

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

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

supporting information, 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

Straightforward Synthesis of Fluorinated Enals via Photocatalytic α-Perfluoroalkenylation of Aldehydes

Wulkesch, Christian,Czekelius, Constantin

, p. 7425 - 7438 (2021/06/21)

(Per)fluorinated substances represent an important compound class with regard to drug design and material chemistry. We found a mild, operationally simple, and inexpensive photocatalytic perfluoroalkenylation reaction giving tetrasubstituted, highly electron-deficient enals straight from aldehydes. This one-step reaction tolerates various functional groups and can be applied to a wide range of substrates giving the products in yields of 52-84%.

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