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2-Dodecylnaphthalene, with the molecular formula C20H24, is an alkylated naphthalene compound characterized by a dodecyl chain attached to the naphthalene ring. It is recognized for its capacity to dissolve a broad spectrum of organic compounds, making it a versatile chemical intermediate and solvent in various industrial applications.

60899-39-0

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60899-39-0 Usage

Uses

Used in Industrial Solvents:
2-Dodecylnaphthalene is used as a solvent for its ability to dissolve a wide range of organic compounds, facilitating its use in the formulation of specialty coatings, adhesives, and industrial lubricants.
Used in Chemical Product Production:
2-Dodecylnaphthalene serves as an intermediate in the synthesis of various chemical products, contributing to the manufacturing process of a diverse array of consumer and industrial goods.
Used in Surfactant and Dispersing Agent Synthesis:
2-Dodecylnaphthalene is utilized as an intermediate in the production of surfactants and dispersing agents, which are essential in industries such as detergents, textiles, and paints for their emulsifying and dispersing properties.
Used in Specialty Coatings:
It is used as a component in specialty coatings, where its solubility properties enhance the performance and durability of the coatings in specific applications.
Used in Adhesive Formulation:
2-Dodecylnaphthalene contributes to the formulation of adhesives, improving their bonding capabilities and performance across different surfaces.
Used in Industrial Lubricants:
2-Dodecylnaphthalene is employed in the manufacturing of industrial lubricants to enhance their lubricating properties and extend the lifespan of machinery components.
Used in Insecticide Production:
2-Dodecylnaphthalene is a component in the production of insecticides, where it may contribute to the effectiveness of these products in controlling pests.
Used in Agricultural Chemicals Manufacturing:
It is also utilized in the manufacturing of agricultural chemicals, potentially aiding in the development of more effective and targeted crop protection products.

Check Digit Verification of cas no

The CAS Registry Mumber 60899-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,9 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60899-39:
(7*6)+(6*0)+(5*8)+(4*9)+(3*9)+(2*3)+(1*9)=160
160 % 10 = 0
So 60899-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H32/c1-2-3-4-5-6-7-8-9-10-11-14-20-17-18-21-15-12-13-16-22(21)19-20/h12-13,15-19H,2-11,14H2,1H3

60899-39-0Downstream Products

60899-39-0Relevant academic research and scientific papers

Switchable Selectivity in the Pd-Catalyzed Alkylative Cross-Coupling of Esters

Masson-Makdissi, Jeanne,Vandavasi, Jaya Kishore,Newman, Stephen G.

, p. 4094 - 4098 (2018/07/15)

The Pd-catalyzed cross-coupling of phenyl esters and alkyl boranes is disclosed. Two reaction modes are rendered accessible in a selective fashion by interchange of the catalyst. With a Pd-NHC system, alkyl ketones can be prepared in good yields via a Suzuki-Miyaura reaction proceeding by activation of the C(acyl)-O bond. Use of a Pd-dcype catalyst enables alkylated arenes to be synthesized by a modified pathway with extrusion of CO. Applications of this divergent coupling strategy and the origin of the switchable selectivity are discussed.

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