3058-01-3 Usage
Description
3-Methyladipic acid, also known as alpha,omega-dicarboxylic acid, is a chemical compound derived from adipic acid with a methyl group substitution at the C-3 position. It is characterized by its white, fine crystalline powder appearance.
Uses
Used in Chemical Synthesis:
3-Methyladipic acid is used as a building block for the synthesis of various chemical compounds, such as polymers, pharmaceuticals, and other specialty chemicals. Its unique structure allows for the creation of novel materials with specific properties tailored for different applications.
Used in Polymer Industry:
3-Methyladipic acid is used as a monomer for the production of polymers with enhanced properties, such as improved mechanical strength, thermal stability, and chemical resistance. These polymers can be utilized in a wide range of applications, including automotive, electronics, and packaging industries.
Used in Pharmaceutical Industry:
3-Methyladipic acid is used as an intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs with potential therapeutic benefits. Its unique chemical structure enables the creation of molecules with specific biological activities, targeting various medical conditions.
Used in Coatings and Adhesives:
3-Methyladipic acid is used as a component in the formulation of coatings and adhesives, providing improved adhesion, durability, and resistance to environmental factors. These coatings and adhesives can be applied in various industries, such as construction, automotive, and aerospace, to enhance the performance and longevity of materials.
Used in Lubricants and Additives:
3-Methyladipic acid is used in the development of lubricants and additives for the automotive, industrial, and marine sectors. Its incorporation into these products can lead to enhanced performance, reduced wear and tear, and improved fuel efficiency, contributing to the overall efficiency and sustainability of various industries.
Synthesis Reference(s)
The Journal of Organic Chemistry, 40, p. 1488, 1975 DOI: 10.1021/jo00898a024
Check Digit Verification of cas no
The CAS Registry Mumber 3058-01-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,5 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3058-01:
(6*3)+(5*0)+(4*5)+(3*8)+(2*0)+(1*1)=63
63 % 10 = 3
So 3058-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O4/c1-5(4-7(10)11)2-3-6(8)9/h5H,2-4H2,1H3,(H,8,9)(H,10,11)/p-2/t5-/m0/s1
3058-01-3Relevant articles and documents
Ozonolysis of methylcyclohexanols and methylcyclohexanones
Syroezhko,Begak
, p. 102 - 105 (2004)
Ozonolysis of isomeric methylcyclohexanols and methylcyclohexanones was studied.
Direct and Selective Synthesis of Adipic and Other Dicarboxylic Acids by Palladium-Catalyzed Carbonylation of Allylic Alcohols
Beller, Matthias,Ge, Yao,Huang, Weiheng,Jackstell, Ralf,Liu, Jiawang,Neumann, Helfried,Yang, Ji
supporting information, p. 20394 - 20398 (2020/09/21)
A general and direct synthesis of dicarboxylic acids including industrially important adipic acid by palladium-catalyzed dicarbonylation of allylic alcohol is reported. Specifically, the combination of PdCl2 and a bisphosphine ligand (HeMaRaphos) promotes two different carbonylation reactions with high activity and excellent selectivity.
Colloidal tectonics for tandem synergistic Pickering interfacial catalysis: Oxidative cleavage of cyclohexene oxide into adipic acid
Yang, Bingyu,Leclercq, Lo?c,Schmitt, Véronique,Pera-Titus, Marc,Nardello-Rataj, Véronique
, p. 501 - 507 (2019/01/10)
Supramolecular preorganization and interfacial recognition can provide useful architectures for colloidal building. To this aim, a novel approach, based on colloidal tectonics involving two surface-active particles containing both recognition and catalytic sites, has been developed for controlling the formation and the properties of Pickering emulsions. This was illustrated by the combination of dodecyltrimethylammonium phosphotungstate nanoparticles, [C12]3[PW12O40], and silica particles functionalized with alkyl and sulfonic acid groups, [Cn/SO3H]@SiO2. The interfacial self-assembly occurs by the penetration of the alkyl chains of [Cn/SO3H]@SiO2 into the [C12]3[PW12O40] supramolecular porous structure constituted of polar and apolar regions. The emulsions were used as a non-nitric acid route for adipic acid synthesis from the one-pot oxidative cleavage of cyclohexene oxide with aqueous H2O2. The catalytic performance was significantly boosted due to the synergistic interactions between the particles.
