15185-37-2 Usage
Uses
Used in Photopolymer Production:
(E)-2-Aminobenzophenone oxime is used as a photoinitiator in the production of photopolymers, facilitating the polymerization process under the influence of light. This application is crucial for the manufacturing of materials with specific properties, such as rapid curing and high performance in various end-use applications.
Used in Material Synthesis:
As a stabilizer, (E)-2-Aminobenzophenone oxime plays a significant role in the synthesis of various materials, enhancing their stability and performance. Its stabilizing properties are particularly valuable in the development of new materials with improved characteristics.
Used in Organic Synthesis as a Reagent:
(E)-2-Aminobenzophenone oxime is utilized as a reagent in organic synthesis, specifically in the formation of Schiff bases, which are important in the synthesis of a wide range of organic compounds. It also plays a role in the preparation of heterocyclic compounds, contributing to the diversity of chemical structures that can be synthesized.
Used in Pharmaceutical Industry:
(E)-2-Aminobenzophenone oxime has potential applications in the pharmaceutical industry, particularly in the development of new drug compounds. Its unique chemical properties and reactivity make it a promising candidate for the creation of innovative pharmaceuticals that can address various medical needs.
Check Digit Verification of cas no
The CAS Registry Mumber 15185-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,8 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15185-37:
(7*1)+(6*5)+(5*1)+(4*8)+(3*5)+(2*3)+(1*7)=102
102 % 10 = 2
So 15185-37-2 is a valid CAS Registry Number.
15185-37-2Relevant academic research and scientific papers
Mild method for the synthesis of 1H-indazoles through oxime-phosphonium ion intermediate
Paul, Saurav,Panda, Subhankar,Manna, Debasis
supporting information, p. 2480 - 2483 (2014/05/06)
The synthesis of 1H-indazoles from o-aminobenzoximes is achieved via N-N bond formation using triphenylphosphine, I2, and imidazole. Selective formation of oxime-phosphonium ion intermediate in the presence of the amino group is the driving for
A practical, metal-free synthesis of 1H-Lndazoles
Counceller, Carla M.,Eichman, Chad C.,Wray, Brertda C.,Stambuli, James P.
supporting information; experimental part, p. 1021 - 1023 (2009/04/07)
The synthesis of 1H-indazoles is achieved from o-aminobenzoximes by the selective activation of the oxime in the presence of the amino group. The reaction occurs with a variety of substituted o-aminobenzoximes using a slight excess of methanesulfonyl chloride and triethylamine at 0-23 °C and is amenable to scale-up. The synthesis of 1 H-indazoles under these conditions is extremely mild compared with previous synthetic approaches and affords the desired compounds in good to excellent yields.
