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6-methylcyclohex-3-ene-1-carboxylic acid is a chemical compound with the molecular formula C8H12O2. It is a carboxylic acid that contains a methyl group and a cyclohexene ring. This versatile compound is known for its potential applications in various fields due to its unique structure.

5406-30-4

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5406-30-4 Usage

Uses

Used in Pharmaceutical Industry:
6-methylcyclohex-3-ene-1-carboxylic acid is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a valuable building block for the development of new molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 6-methylcyclohex-3-ene-1-carboxylic acid serves as an intermediate in the synthesis of various agrochemicals. Its role in creating new molecules contributes to the development of innovative products for agricultural use.
Used in Research and Development:
6-methylcyclohex-3-ene-1-carboxylic acid is utilized as a building block in research and development for the production of new molecules with potential applications in various industries. Its versatility in chemical reactions makes it a valuable tool in the field of organic chemistry.
Used in Organic Chemistry:
As a carboxylic acid with a methyl group and a cyclohexene ring, 6-methylcyclohex-3-ene-1-carboxylic acid is a valuable compound in organic chemistry. Its structure makes it suitable for various chemical reactions, contributing to the synthesis of a wide range of organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 5406-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5406-30:
(6*5)+(5*4)+(4*0)+(3*6)+(2*3)+(1*0)=74
74 % 10 = 4
So 5406-30-4 is a valid CAS Registry Number.

5406-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methylcyclohex-3-ene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names trans-2-methylcyclohex-2-ene carboxylic acid

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:5406-30-4 SDS

5406-30-4Relevant academic research and scientific papers

The design of a new ZrO2-supported V/P/O catalyst for n-butane oxidation to maleic anhydride: The build-up of the active phase during thermal treatment

Caldarelli,Cavani,Folco,Luciani,Cortelli,Leanza

experimental part, p. 204 - 210 (2011/01/04)

This study concerns the generation of the active V/P/O phase in supported catalysts used for n-butane oxidation to maleic anhydride. Catalysts were prepared by impregnating a zirconia support with ammonium vanadate and phosphoric acid, with subsequent thermal treatment under various environments and temperatures. The catalysts were studied by means of in situ Raman spectroscopy and reactivity measurements. It was found that the nature of the active surface is greatly affected both by the composition of the gas phase used for the thermal treatment, and by the P/V ratio used for catalyst preparation. δ-VOPO4 was initially formed by the high-temperature reaction of vanadium salt with phosphoric acid; however, in the sample prepared with only 10% excess phosphorus (P/V atomic ratio = 1.1), δ-VOPO4 transformed into either V2O5, in a steam-enriched air stream, or αII- and β-VOPO4, in a dry air stream. δ-VOPO4 was more stable in the sample prepared with a large excess of P, i.e., with P/V = 1.3 and 1.5. The latter catalyst showed the best catalytic performance in n-butane oxidation. However, the performance was worse than that of the commercial unsupported vanadyl pyrophosphate catalyst.

STUDIES OF COMPOUNDS IN THE MENTHANE SERIES. XIX. SYNTHESIS AND PROPERTIES OF TRANS-o-4-MENTHEN-8-OL AND STEREOISOMERIC o-5-METHEN-8-OLS

Bazyl'chik, V. V.,Fedorov, P. I.,Klyuev, N. A.,Dank, E. Kh.

, p. 1320 - 1327 (2007/10/02)

Trans-o-4-Menthen-8-ol and cis- and trans-o-5-menthen-8-ols have been prepared via the Diels-Alder reactions of 1,3-butadiene with crotonaldehyde in the presence of boron trifluoride etherate, and piperylene with methyl acrylate, respectively.The dehydration reactions of these alcohols have been studied in the presence of acetic anhydride and potassium bisulfate; the latter reagent demonstrates a high reaction selectivity.

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