4074-23-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
1,3,5-Trimethyl-1,4-cyclohexadiene is used as a chemical intermediate in the synthesis of pharmaceuticals and agrochemicals. Its role in these industries is crucial for the production of various drugs and agricultural chemicals, contributing to advancements in healthcare and agriculture.
Used in Paints, Varnishes, and Adhesives Industry:
As a solvent, 1,3,5-trimethyl-1,4-cyclohexadiene is utilized in the paints, varnishes, and adhesives industry. Its solvent properties aid in the manufacturing process, ensuring the desired consistency and performance of these products.
Used in Fragrance Production:
1,3,5-Trimethyl-1,4-cyclohexadiene is also used in the production of fragrances, where it contributes to the creation of various scent profiles for different applications, such as perfumes, cosmetics, and other scented products.
Used in Dyes and Pigments Manufacturing:
In the manufacturing of dyes and pigments, 1,3,5-trimethyl-1,4-cyclohexadiene serves as a chemical intermediate. Its involvement in this process is essential for developing a wide range of colorants used in various industries, including textiles, plastics, and printing.
Safety Considerations:
Given that 1,3,5-trimethyl-1,4-cyclohexadiene is considered hazardous, it is imperative to follow proper safety measures when handling and storing 1,3,5-TRIMETHYL-1,4-CYCLOHEXADIENE. This ensures the protection of individuals and the environment from potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 4074-23-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4074-23:
(6*4)+(5*0)+(4*7)+(3*4)+(2*2)+(1*3)=71
71 % 10 = 1
So 4074-23-1 is a valid CAS Registry Number.
4074-23-1Relevant articles and documents
Desymmetrization of cyclohexa-1,4-dienes - A straightforward route to cyclic and acyclic polyhydroxylated systems
Landais, Yannick,Zekri, Elisabeth
, p. 4037 - 4053 (2007/10/03)
A straightforward route to polyols, amino polyols, polysubstituted lactols and lactones from readily available arenes has been devised. It uses a three- or four-step sequence involving a Birch reduction of the arene, followed by desymmetrization through d
Desymmetrisation and ring opening of cyclohexa-1,4-dienes. An access to highly functionalised cyclic and acyclic systems
Landais, Yannick,Zekri, Elisabeth
, p. 6547 - 6551 (2007/10/03)
Acyclic and cyclic synthons are readily available in three steps starting from substituted arenes. Birch reduction of the latter followed by desymmetrisation through Sharpless AD reaction then ozonolysis thus afforded five-membered ring lactols and acycli
