7154-10-1 Usage
Description
[4-(propan-2-yl)phenyl]methanediyl diacetate, also known as diacetone diperoxide, is an organic compound characterized by its molecular formula C11H18O4. It is a peroxide compound that is recognized for its use as a polymerization initiator and a bleaching agent across various industries. Notably, diacetone diperoxide is known for its highly explosive properties, necessitating extreme caution in handling and storage.
Uses
Used in Plastics Industry:
In the plastics industry, [4-(propan-2-yl)phenyl]methanediyl diacetate is utilized as a polymerization initiator. Its role is crucial in the production process, facilitating the formation of polymer chains and enhancing the overall efficiency of the process.
Used in Rubber Industry:
Similarly, in the rubber industry, [4-(propan-2-yl)phenyl]methanediyl diacetate serves as a polymerization initiator. It aids in the creation of rubber polymers, contributing to the development of rubber products with specific properties tailored to various applications.
Used in Adhesives Production:
[4-(propan-2-yl)phenyl]methanediyl diacetate is also employed in the production of adhesives. As a polymerization initiator, it helps in the synthesis of adhesive polymers, ensuring the creation of strong and durable bonding agents.
Used in Organic Compounds Synthesis:
Furthermore, [4-(propan-2-yl)phenyl]methanediyl diacetate is used in the synthesis of other organic compounds. Its reactivity and properties make it a valuable intermediate in the production of various chemicals and substances.
Used as a Bleaching Agent:
In addition to its role as a polymerization initiator, [4-(propan-2-yl)phenyl]methanediyl diacetate is also used as a bleaching agent in different industries. Its ability to oxidize and lighten substances makes it suitable for applications where color removal or lightening is required.
Check Digit Verification of cas no
The CAS Registry Mumber 7154-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7154-10:
(6*7)+(5*1)+(4*5)+(3*4)+(2*1)+(1*0)=81
81 % 10 = 1
So 7154-10-1 is a valid CAS Registry Number.
7154-10-1Relevant articles and documents
Application of poly(Vinylbenzyltrimethylammonium tribromide) resin as an efficient polymeric catalyst in the acetalization and diacetylation of benzaldehydes
Han, Bingbing,Hu, Junjun,Li, Xianwei,Zheng, Zubiao
supporting information, p. 287 - 293 (2021/04/28)
The applications of a new supported tribromide reagent (poly(vinylbenzyltrimethylammonium tribromide) resin) were reported. This supported tribromide resin was used as a catalyst in the acetalization and diacetylation of benzaldehydes under mild conditions with high efficiency. The effects of solvents, and amount of the supported tribromide resin on the reactions were investigated. Under the optimal conditions, most of acetal and 1,1-diacetates of benzaldehydes were selectively obtained in excellent yields.
Green procedures for the chemoselective synthesis of acylals and their cleavage promoted by recoverable sulfonic acid based nanoporous carbon (CMK-5-SO3H)
Zareyee, Daryoush,Mirzajanzadeh, Ehsan,Khalilzadeh, Mohammad Ali
, p. 1229 - 1234 (2015/10/06)
A selective synthesis of gem-diacetates from the reaction of aldehydes and acetic anhydride in the presence of recyclable nanoporous solid sulfonic acid (CMK-5-SO3H) under solvent-free reaction conditions is reported. The catalyst was also found to be highly active for deprotection of resulting acylals in water. [Figure not available: see fulltext.]
Lithium trifluoromethanesulfonate (LiOTf) as a recyclable catalyst for highly efficient acetylation of alcohols and diacetylation of aldehydes under mild and neutral reaction conditions
Karimi, Babak,Maleki, Jafar
, p. 4951 - 4954 (2007/10/03)
A variety of alcohols and aldehydes were reacted with acetic anhydride at room temperature in the presence of a catalytic amount of lithium triflate (LiOTf) to produce the corresponding esters and 1,1-diacetates, respectively, in good to excellent yields under essentially neutral reaction conditions. Sensitive functional groups such as PhCO2-, OMe, and OTBDMS ethers survived intact under the described reaction conditions.
