446864-55-7 Usage
Uses
Used in Pharmaceutical Industry:
2-Bromo-3-formylbenzonitrile is used as a key intermediate in the synthesis of various pharmaceuticals. Its reactivity allows for the creation of new compounds with potential therapeutic properties, contributing to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-3-formylbenzonitrile serves as a crucial component in the production of certain agrochemicals. Its ability to participate in chemical reactions enables the synthesis of compounds that can be used in pest control and crop protection.
Used in Organic Synthesis:
2-Bromo-3-formylbenzonitrile is utilized as a versatile building block in organic synthesis. It is employed for the preparation of a variety of organic compounds, leveraging its reactivity to form new molecules with specific functionalities and applications.
The precise applications and uses of 2-Bromo-3-formylbenzonitrile are contingent upon the specific synthetic and processing conditions in which it is used, highlighting its adaptability in diverse chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 446864-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,6,8,6 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 446864-55:
(8*4)+(7*4)+(6*6)+(5*8)+(4*6)+(3*4)+(2*5)+(1*5)=187
187 % 10 = 7
So 446864-55-7 is a valid CAS Registry Number.
446864-55-7Relevant articles and documents
Synthesis and structure-activity relationships of novel benzoxaboroles as a new class of antimalarial agents
Zhang, Yong-Kang,Plattner, Jacob J.,Freund, Yvonne R.,Easom, Eric E.,Zhou, Yasheen,Gut, Jiri,Rosenthal, Philip J.,Waterson, David,Gamo, Francisco-Javier,Angulo-Barturen, Inigo,Ge, Min,Li, Zhiya,Li, Lingchao,Jian, Yong,Cui, Han,Wang, Hailong,Yang, Jian
, p. 644 - 651 (2011/03/18)
A series of boron-containing benzoxaborole compounds was designed and synthesized for a structure-activity relationship investigation surrounding 7-(HOOCCH2CH2)-1,3-dihydro-1-hydroxy-2,1-benzoxaborole (1) with the goal of discovering
One-pot tandem decarboxylative allylation-heck cyclization of allyl diphenylglycinate imines: Rapid access to polyfunctionalized 1-aminoindanes
Fields, Wendy H.,Khan, Ali K.,Sabat, Michal,Chruma, Jason J.
supporting information; experimental part, p. 5131 - 5134 (2009/05/30)
(Figure Presented) 1-Aminoindanes are generated from allyl diphenylglycinate imines employing a one-pot palladium-catalyzed decarboxylative allylation-Hecyclization cascade. Variation of both the aryl and allyl moieties leads to a diverse range of polycyclic imines, amenable to the synthesis natural products and other biologically relevant small molecules.
