18802-67-0 Usage
Uses
Used in Pharmaceutical Industry:
[(4-chlorobenzylidene)amino]oxy(phenyl)methanone is used as a potential candidate for pharmaceutical applications due to its unique functional groups and complex structure. The presence of the amino and methanone groups may allow for interactions with biological targets, making it a compound of interest for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, [(4-chlorobenzylidene)amino]oxy(phenyl)methanone can be used as a starting material or intermediate for the synthesis of more complex molecules. Its unique structure and functional groups may facilitate the development of novel chemical compounds with specific properties and applications.
Used in Material Science:
[(4-chlorobenzylidene)amino]oxy(phenyl)methanone may also find applications in material science, where its unique structure and functional groups could be exploited to create new materials with tailored properties. Further research is required to understand its potential in this field.
Used in Dye and Pigment Industry:
Given its complex structure and the presence of a phenyl group, [(4-chlorobenzylidene)amino]oxy(phenyl)methanone could potentially be used in the development of new dyes and pigments. [(4-chlorobenzylidene)amino]oxy(phenyl)methanone's specific functional groups may contribute to the color and stability of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 18802-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,0 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18802-67:
(7*1)+(6*8)+(5*8)+(4*0)+(3*2)+(2*6)+(1*7)=120
120 % 10 = 0
So 18802-67-0 is a valid CAS Registry Number.
18802-67-0Relevant articles and documents
Iron-catalyzed synthesis of benzoxazoles by oxidative coupling/cyclization of phenol derivatives with benzoyl aldehyde oximes
Gao, Sen,Gao, Liming,Meng, Hong,Luo, Meiming,Zeng, Xiaoming
, p. 9886 - 9889 (2017/09/11)
An iron-catalyzed oxidative coupling/cyclization reaction for the synthesis of benzoxazoles at room temperature is reported. This reaction was enabled by an inexpensive iron(iii) catalyst by treating readily available phenol derivatives with benzoyl aldehyde oximes. Mechanistic studies show that benzoyl aldehyde oxime is not only used as a substrate, but also serves as an ancillary ligand to support the iron salt in the promotion of the transformation.
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.
