6337-69-5 Usage
Description
(2E)-N-hydroxy-1,1-diphenylpropan-2-imine is a hydroxylamine derivative with the molecular formula C15H15NO. It is a chemical compound that serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a versatile compound with potential applications in various fields of chemistry and medicine.
Uses
Used in Organic Synthesis:
(2E)-N-hydroxy-1,1-diphenylpropan-2-imine is used as a reagent in organic synthesis for the preparation of various compounds.
Used in Pharmaceutical Industry:
(2E)-N-hydroxy-1,1-diphenylpropan-2-imine is used as a key intermediate in the synthesis of various pharmaceuticals for its potential therapeutic applications.
Used in Agrochemical Industry:
(2E)-N-hydroxy-1,1-diphenylpropan-2-imine is used as a key intermediate in the synthesis of various agrochemicals for its potential applications in agriculture.
Used in Specialty Chemicals:
(2E)-N-hydroxy-1,1-diphenylpropan-2-imine is used as a key intermediate in the synthesis of various specialty chemicals for its unique properties and reactivity.
Used as a Radical Scavenger and Antioxidant:
(2E)-N-hydroxy-1,1-diphenylpropan-2-imine has been investigated for its potential use as a radical scavenger and antioxidant due to its unique structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 6337-69-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6337-69:
(6*6)+(5*3)+(4*3)+(3*7)+(2*6)+(1*9)=105
105 % 10 = 5
So 6337-69-5 is a valid CAS Registry Number.
6337-69-5Relevant articles and documents
Modular 2,3-diaryl-2: H -azirine synthesis from ketoxime acetates via Cs2CO3-mediated cyclization
Zhao, Mi-Na,Zhang, Wei,Wang, Xu-Cai,Zhang, Ying,Yang, De-Suo,Guan, Zheng-Hui
supporting information, p. 4333 - 4337 (2018/06/21)
A modular 2H-azirine synthesis from ketoxime acetates via Cs2CO3-mediated cyclization has been developed. The reaction utilizes easily available starting materials and provides a general synthetic route to 2,3-diaryl-2H-azirines in good to excellent yields under mild conditions, which is complementary to the conventional approaches for the synthesis of 2H-azirines. A gram-scale reaction was performed to demonstrate the scale-up applicability of this synthetic method. Importantly, 2H-azirines can be efficiently converted to various azaheterocycles.
The Neber route to substituted indoles
Taber, Douglass F.,Tian, Weiwei
, p. 1058 - 1059 (2007/10/03)
Two complementary procedures have been developed for the conversion of the oximes of α-aryl ketones to azirines. On heating, the azirines rearrange smoothly to the corresponding indoles. The overall transformation offers a versatile route to indoles, complementary to the Fischer indole synthesis. Copyright
TITANIUM TRICHLORIDE MEDIATED REDUCTION OF NITROSTYRENES
Sera, Akira,Fukumoto, Shoji,Yoneda, Takako,Yamada, Hiroaki
, p. 697 - 702 (2007/10/02)
Reactions of substituted nitrostyrenes with aqueous titanium trichloride afforded pyrroles, carbonyl compounds, and oximes.In some instances, divinylamines were produced as well.The reaction mechanism is rationalized taking account of electron transfer to nitroethylenes from Ti(III), followed by protonation, dimerization, cyclization, and hydrolysis.
