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4-Methylcyclohexane-1,2-dione, also known as 4-methyl-1,2-cyclohexanedione, is an organic compound with the chemical formula C7H10O2. It is a white crystalline solid that is soluble in organic solvents. 4-Methylcyclohexane-1,2-dione is a derivative of cyclohexane, with a methyl group attached to the fourth carbon and two carbonyl groups (C=O) at the first and second carbons. 4-Methylcyclohexane-1,2-dione is used as an intermediate in the synthesis of various chemicals, including pharmaceuticals and agrochemicals. It is also known for its potential applications in the production of fragrances and flavorings. The compound is synthesized through various methods, such as the oxidation of 4-methylcyclohexanol or the condensation of acetone with acetoacetic ester. Due to its reactivity, it is important to handle 4-methylcyclohexane-1,2-dione with care, as it may be harmful if inhaled, ingested, or absorbed through the skin.

3008-42-2

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3008-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3008-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3008-42:
(6*3)+(5*0)+(4*0)+(3*8)+(2*4)+(1*2)=52
52 % 10 = 2
So 3008-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O2/c1-5-2-3-6(8)7(9)4-5/h5H,2-4H2,1H3

3008-42-2SDS

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 4-methyl-1,2-cyclohexanedione

1.2 Other means of identification

Product number -
Other names 4-METHYLCYCLOHEXANE-1,2-DIONE

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:3008-42-2 SDS

3008-42-2Relevant academic research and scientific papers

Process for preparing 4-substituted-1H-indole-3-glyoxamides

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, (2008/06/13)

A process for preparing 1H-indole-3-glyoxamides useful for inhibiting SPLA2 and novel intermediates useful in the preparation of such compounds.

Process for preparing 4-substituted-1H-indole-3-glyoxamides

-

, (2008/06/13)

A process for preparing 1H-indole-3-glyoxamides useful for inhibiting SPLA2 and novel intermediates useful in the preparation of such compounds.

REGIOSELECTIVE REDUCTIONS OF 2,3-EPOXY ACETALS WITH ZINC-CHLOROTRIMETHYLSILANE AND LITHIUM ALUMINIUM HYDRIDE: CONVENIENT SYNTHESIS OF 1,2 AND 1,3-DIONES

Vankar, Yashwant D.,Chaudhuri, Narayan C.,Rao, C. Trinadha

, p. 551 - 554 (2007/10/02)

A variety of 2,3-epoxy acetals have been found to undergo regioselective reductions with zinc-chlorotrimethylsilane and lithium aluminium hydride to give 2-hydroxy and 3-hydroxy acetals respectively.Their oxidation followed by hydrolysis furnished the corresponding 1,2- and 1,3-diones in good yields.

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