1417567-41-9 Usage
General Description
1-Bromo-3-chloro-5-(trifluoromethoxy)benzene is a chemical compound that integrates several types of atoms, including hydrogen, carbon, chlorine, bromine, and fluorine. It belongs to the category of organobromides and specifically to the subcategory of aryl bromides. With its nine carbon atoms, it represents a form of aromatic organohalogen compound. Bromine and chlorine atoms are included in the structure as halogens. There are three fluorine atoms encompassed in a trifluoromethoxy group replacing a hydrogen atom in the benzene ring. The presence of various atoms grants the compound good stability and versatility, potentially making it useful in chemical research and pharmaceutical studies. However, its specific physical properties such as its boiling point, density, and melting point, as well as potential usages, depend on further investigations.
Check Digit Verification of cas no
The CAS Registry Mumber 1417567-41-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,5,6 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1417567-41:
(9*1)+(8*4)+(7*1)+(6*7)+(5*5)+(4*6)+(3*7)+(2*4)+(1*1)=169
169 % 10 = 9
So 1417567-41-9 is a valid CAS Registry Number.
1417567-41-9Relevant articles and documents
Silver-Mediated Trifluoromethoxylation of (Hetero)aryldiazonium Tetrafluoroborates
Yang, Yu-Ming,Yao, Jian-Fei,Yan, Wei,Luo, Zhuangzhu,Tang, Zhen-Yu
, p. 8003 - 8007 (2019)
Here we report a silver-mediated trifluoromethoxylation of (hetero)aryldiazonium tetrafluoroborates by converting an aromatic amino group into an OCF3 group. This method, which can be considered to be a trifluoromethoxylation variation of the classic Sandmeyer-type reaction, uses readily available aryl and heteroaromatic amines as starting materials and AgOCF3 as trifluoromethoxylating reagents. The broad substrate scope and simple, mild reaction condition made this transformation a valuable method in constructing aryl-OCF3 bonds.
