74421-03-7 Usage
Uses
Used in Polymer Production:
2,4-Dimethyl-2-decene is utilized as a monomer in the synthesis of polymers, contributing to the formation of polymers with specific properties tailored for various applications.
Used in Organic Synthesis:
As a precursor, 2,4-Dimethyl-2-decene is employed in the synthesis of a range of organic compounds, leveraging its reactive double bond and branched structure to produce diverse chemical entities.
Used as a Reagent in Organic Chemistry:
Owing to its specific molecular structure, 2,4-Dimethyl-2-decene serves as a reagent in various organic chemistry reactions, facilitating targeted transformations and the formation of desired products.
Used in the Plastics Industry:
2,4-Dimethyl-2-decene finds application in the production of plastics, where its incorporation influences the material properties, such as flexibility, strength, and durability.
Used in the Adhesives Industry:
In the formulation of adhesives, 2,4-Dimethyl-2-decene enhances the bonding properties, providing improved adhesion and resistance to various environmental conditions.
Used in the Coatings Industry:
2,4-Dimethyl-2-decene is also utilized in the production of coatings, where it contributes to the development of coatings with specific characteristics, such as resistance to wear, UV stability, and aesthetic appeal.
Check Digit Verification of cas no
The CAS Registry Mumber 74421-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,2 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74421-03:
(7*7)+(6*4)+(5*4)+(4*2)+(3*1)+(2*0)+(1*3)=107
107 % 10 = 7
So 74421-03-7 is a valid CAS Registry Number.
74421-03-7Relevant articles and documents
Iron-catalyzed alkylation of alkenyl grignard reagents
Cahiez, Gerard,Duplais, Christophe,Moyeux, Alban
, p. 3253 - 3254 (2007)
The first iron-catalyzed cross-coupling reaction between alkenyl Grignard reagents and n- or s-alkyl bromides is described. The reaction is stereoselective and takes place in the presence of 5 mol % of [Fe(acac) 3MEDA/HMTA] (1:2:1) under very mild conditions (THF, 0°C, 45 min).
