942-89-2 Usage
Uses
Used in Chemical Industry:
Acetoxime benzoate is used as a solvent and intermediate for the production of perfumes, pharmaceuticals, and other organic compounds. Its ability to react with other chemicals to form new compounds makes it a valuable asset in the synthesis of a wide range of products.
Used in Plastics Manufacturing:
Acetoxime benzoate is used as a stabilizer and inhibitor in the manufacture of plastics. Its presence helps to prevent the degradation of plastic materials, thereby enhancing their durability and performance.
Used in Adhesives Production:
In the adhesives industry, acetoxime benzoate serves as a stabilizer and inhibitor, ensuring the stability and longevity of adhesive products. Its use contributes to the development of high-quality adhesives with improved bonding properties.
Used in Coatings Industry:
Acetoxime benzoate is utilized as a stabilizer and inhibitor in the production of coatings. Its incorporation into coating formulations helps to maintain the integrity and performance of the coatings, providing protection and durability to various surfaces.
Safety Precautions:
While acetoxime benzoate offers numerous benefits in various industries, it is essential to handle it with care due to its potential hazards. Proper safety measures should be taken to minimize risks associated with its use, ensuring the safety of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 942-89-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 942-89:
(5*9)+(4*4)+(3*2)+(2*8)+(1*9)=92
92 % 10 = 2
So 942-89-2 is a valid CAS Registry Number.
942-89-2Relevant academic research and scientific papers
A novel synthesis of carboxylic acid oxime esters catalyzed by 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate
Shi, Wei,Zhang, Jiming,Zhou, Qin,Wang, Xingjian,Qi, Xiaowei,Guo, Lianyong,Ma, Wanyong,Zhou, Jianhua
, p. 7125 - 7128 (2015/04/22)
We describe a facile synthesis of carboxylic acid oxime esters in acetonitrile from the corresponding carboxylic acids and oximes catalyzed by 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate in the presence of triethylamine at room temperature under mild conditions.
Te-1-acylmethyl and Te-1-iminoalkyl telluroesters: Synthesis and thermolysis leading to 1,3-diketones and O-alkenyl and O-imino esters
Nakaiida, Shoho,Kato, Shinzi,Niyomura, Osamu,Ishida, Masaru,Ando, Fumio,Koketsu, Jugo
experimental part, p. 930 - 946 (2010/08/04)
A series of Te-1-acylmethyl carbotelluroates was prepared in good isolated yields from the reaction of potassium carbotelluroates with -haloketones in acetonitrile. Thermolysis of the telluroesters afforded vinyl esters in 20-50% yields, while treatment of the carbotellurorates with potassium t-butanolate led to 1,3-diketones in 30-75% yields with the liberation of black tellurium. The reaction of potassium carbotelluroates with -haloaceto oximes gave O-acyl oximes in 50-70% yields via Te-1-iminomethylcarbotelluroates. Copyright Taylor & Francis Group.
Reaction of Trimethylsilyl Azide with C=N-O Bond
Nishiyama, Kozaburo,Miyata, Izumi
, p. 2419 - 2420 (2007/10/02)
Trimethylsilyl azide (TMSA) was reacted with an oxime ester or a Reissert salt in the presence of trimethylsilyl trifluoromethanesulfonate to give tetrazole derivative.The details of these reactions are examined.
