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4351-02-4

2,2,6-Trimethyl-cyclohexanecarboxylic acid is an organic compound with the molecular formula C??H??O?. It is a derivative of cyclohexane, featuring a carboxylic acid functional group attached to the cyclohexane ring. The molecule has three methyl groups (CH?) attached to the cyclohexane ring, with two methyl groups at the 2-position and one at the 6-position. 2,2,6-trimethyl-cyclohexanecarboxylic acid is a white crystalline solid and is known for its potential use in the synthesis of various pharmaceuticals and chemical intermediates. It is also used in the production of certain fragrances and flavorings. The compound's structure provides it with unique chemical properties, making it a valuable component in various industrial applications.

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  • 4351-02-4 Structure

  • Basic information

    1. Product Name: 2,2,6-trimethyl-cyclohexanecarboxylic acid
    2. Synonyms: 2,2,6-trimethyl-cyclohexanecarboxylic acid
    3. CAS NO:4351-02-4
    4. Molecular Formula:
    5. Molecular Weight: 170.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4351-02-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2,6-trimethyl-cyclohexanecarboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2,6-trimethyl-cyclohexanecarboxylic acid(4351-02-4)
    11. EPA Substance Registry System: 2,2,6-trimethyl-cyclohexanecarboxylic acid(4351-02-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 4351-02-4(Hazardous Substances Data)

4351-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4351-02-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4351-02:
(6*4)+(5*3)+(4*5)+(3*1)+(2*0)+(1*2)=64
64 % 10 = 4
So 4351-02-4 is a valid CAS Registry Number.

4351-02-4Relevant articles and documents

Gold supported on a mesoporous CeO2 matrix as an efficient catalyst in the selective aerobic oxidation of aldehydes in the liquid phase

Corma, Avelino,Domine, Marcelo E.

, p. 4042 - 4044 (2005)

Gold supported on CeO2 catalyses the selective aerobic oxidation of aliphatic and aromatic aldehydes better than other reported catalysts such as Pt/C/Bi materials; the activity is due to the nanometric particle size of Au and CeO2. The Royal Society of Chemistry 2005.

PROCESS FOR MANUFACTURING A SUBSTITUTED CYCLOHEXANECARBONITRILE

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Page/Page column 10; 11, (2021/03/19)

A process for manufacturing a substituted cyclohexanecarbonitrile said process comprising the following steps: - reacting the corresponding substituted cyclohexanecarboxylic acid with thionyl chloride to make the corresponding acyl chloride; and simultaneously or subsequently - reacting the chloride with sulfonamide in sulfolane as solvent to make the substituted cyclohexanecarbonitrile.

OPSIN-BINDING LIGANDS, COMPOSITIONS AND METHODS OF USE

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Page/Page column 163-164, (2010/12/31)

Compounds and compositions of said compounds along with methods of use of compounds are disclosed for treating ophthalmic conditions related to mislocalization of opsin proteins, the misfolding of mutant opsin proteins and the production of toxic visual cycle products that accumulate in the eye. Compounds and compositions useful in the these methods, either alone or in combination with other therapeutic agents, are also described.

Ethyl (1R,6S)-2,2,6-trimethylcyclohexanecarboxylate, aroma chemical composition containing the same and process of producing the same

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, (2008/06/13)

Ethyl (1R,6S)-2,2,6-trimethylcyclohexanecarboxylate represented by formula (1) STR1 is disclosed. Also, an aroma chemical composition containing the same and a process of the production of the same are disclosed.

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