80438-65-9 Usage
Uses
Used in Chemical Production:
2,4-di-tert-butyl-1-chlorobenzene is used as a starting material for the synthesis of various other chemicals and pharmaceuticals, leveraging its unique structure to facilitate the creation of a range of compounds.
Used in Organic Synthesis:
As a solvent, 2,4-di-tert-butyl-1-chlorobenzene is utilized in organic synthesis processes, providing a medium that supports the reactions necessary for the production of desired organic compounds.
Used in Plastics and Rubber Manufacturing:
In the plastics and rubber industry, 2,4-di-tert-butyl-1-chlorobenzene is used as a component in the manufacturing process, contributing to the development of materials with specific properties required for various applications.
Used in Dye Production:
2,4-di-tert-butyl-1-chlorobenzene is also employed in the production of dyes, where its chemical structure plays a role in imparting color and stability to the final products.
Used in Agriculture:
2,4-di-tert-butyl-1-chlorobenzene has applications in the agricultural sector as a pesticide, highlighting its versatility and effectiveness in controlling pests that can damage crops.
Used in High-Performance Polymers:
2,4-di-tert-butyl-1-chlorobenzene is also used in the production of high-performance polymers, where its properties contribute to the development of materials with enhanced characteristics suitable for specialized applications.
Check Digit Verification of cas no
The CAS Registry Mumber 80438-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,3 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80438-65:
(7*8)+(6*0)+(5*4)+(4*3)+(3*8)+(2*6)+(1*5)=129
129 % 10 = 9
So 80438-65-9 is a valid CAS Registry Number.
80438-65-9Relevant academic research and scientific papers
REACTIONS OF DI- AND TRI-TERT-BUTYLCYCLOPENTADIENES WITH DIHALOCARBENES
Dehmlow, Eckehard V.,Bollmann, Christof
, p. 3755 - 3758 (2007/10/02)
Dihalocarbene additions to mixed 1,3- and 1,4-di-tert-butylcyclopentadienes (1, 3) allow to prepare 1,3-di-tert-butyl-4-halobenzenes (9) in an efficient way.Only the 3,4 double bond is attacked regiospecifically in 1,3,5-tri-tert-butylcyclopentadiene (11) (and also in 1).Totally unexpected main products from 11 are compounds 9 again being formed under fragmentation of a tert-butyl group.Only small amounts of 1,2,4-tri-tert-butyl-5-halobenzenes (13, X=Cl, Br) are obtained from 11.A labile primary dichlorocarbene adduct to 11 (12a) can be isolated.Its thermal decomposition occurs with the loss of one tert-butyl group to yield 9a.Base catalyzed degradation of 12a gives 9a and 13a as by-product.
Derivatives of m-di-tert-butylbenzene. Part VI. The preparation of miscellaneous halogenated compounds
Koning, Adrianus Jan de
, p. 421 - 425 (2007/10/02)
The preparation of seven series of dihalogenated and monohalogenated derivatives of m-di-tert-butylbenzene, comprising twenty three new compounds, is described.
