55170-80-4 Usage
Uses
Used in Chemical Synthesis:
2,4-Dimethyl-1-decene is used as an intermediate and building block for the synthesis of various organic compounds, such as polymers, resins, and pharmaceuticals. Its versatility in chemical reactions allows for the creation of a diverse range of products.
Used in Solvent Applications:
2,4-Dimethyl-1-decene is utilized as a solvent in various industrial processes due to its ability to dissolve a wide range of substances, facilitating chemical reactions and improving process efficiency.
Used in Specialty Chemicals Production:
2,4-Dimethyl-1-decene is used as a component in the production of specialty chemicals, where its unique properties contribute to the development of high-performance materials with specific applications.
Used in Surfactant Manufacturing:
In the surfactant industry, 2,4-Dimethyl-1-decene is used as a key ingredient in the formulation of surfactants, which are essential in various applications such as detergents, emulsifiers, and wetting agents.
Used in Lubricant Formulation:
2,4-Dimethyl-1-decene is employed in the formulation of lubricants, where its properties help improve the performance and efficiency of lubricating oils in various mechanical systems.
Used in Plasticizer Production:
In the plasticizer industry, 2,4-Dimethyl-1-decene is used to produce plasticizers that enhance the flexibility and workability of plastics, making them suitable for a wide range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 55170-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,7 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55170-80:
(7*5)+(6*5)+(5*1)+(4*7)+(3*0)+(2*8)+(1*0)=114
114 % 10 = 4
So 55170-80-4 is a valid CAS Registry Number.
55170-80-4Relevant academic research and scientific papers
Silver-catalyzed benzylation and allylation reactions of tertiary and secondary alkyl halides with grignard reagents
Someya, Hidenori,Ohmiya, Hirohisa,Yorimitsu, Hideki,Oshima, Koichiro
scheme or table, p. 969 - 971 (2009/04/10)
Treatment of alkyl halides, including tertiary alkyl bromides, with benzylic or allylic Grignard reagent in the presence of a catalytic amount of silver nitrate in ether yielded the corresponding cross-coupling products in high yields. The coupling reactions of tertiary alkyl halides provide efficient access to quaternary carbon centers.
BIS(ALK-4-ENYL)ZINK-VERBINDUNGEN DURCH ADDITION VON ALK-2-ENYLZINK AN OLEFINE
Lehmkuhl, Herbert,Doering, Ingo,Nehl, Hans
, p. 123 - 130 (2007/10/02)
The dialk-2-enylzinc compounds I-IV add to ethylene, oct-1-ene and 3,3-dimethylcyclopropene to give the corresponding di-alk-4-enylzinc compounds VI-IX (88-98percent yield), XV and XVI (90-94percent yield), XVII (7percent) and XXIIIa-XXVIa (91-98percent yield).Additions to XIII are regioselective with Zn -> C(1) while stereoselective cis-addition to XXII is observed.
