831203-34-0 Usage
Description
(Z)-tert-Butyl 2-(5-bromopyridin-2(1H)-ylidene)-2-cyanoacetate is an alpha-diketo compound that is a derivative of pyridinone with a molecular formula of C14H15BrN2O2. It belongs to the class of organic compounds known as alpha-diketo compounds.
Used in Chemical Research:
(Z)-tert-Butyl 2-(5-bromopyridin-2(1H)-ylidene)-2-cyanoacetate is used as a research chemical for experimental purposes in the field of chemistry. Its unique chemical properties make it valuable for studying various chemical reactions and processes.
Used in Pharmaceutical Development:
(Z)-tert-Butyl 2-(5-bromopyridin-2(1H)-ylidene)-2-cyanoacetate is used as a building block in the development and study of pharmaceuticals and other biologically active substances. Its unique structure and properties contribute to the creation of new drugs and therapeutic agents.
Used in Synthesis of Biologically Active Substances:
(Z)-tert-Butyl 2-(5-bromopyridin-2(1H)-ylidene)-2-cyanoacetate is used as a key intermediate in the synthesis of biologically active substances. Its presence in the molecular structure can impart specific biological activities, making it a useful component in the development of new compounds with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 831203-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,1,2,0 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 831203-34:
(8*8)+(7*3)+(6*1)+(5*2)+(4*0)+(3*3)+(2*3)+(1*4)=120
120 % 10 = 0
So 831203-34-0 is a valid CAS Registry Number.
831203-34-0Relevant articles and documents
Synthesis and structure-activity relationship studies of highly potent novel oxazolidinone antibacterials
Komine, Takashi,Kojima, Akihiko,Asahina, Yoshikazu,Saito, Tatsuhiro,Takano, Hisashi,Shibue, Taku,Fukuda, Yasumichi
supporting information; experimental part, p. 6558 - 6562 (2009/10/23)
Novel antibacterial biaryl oxazolidinones bearing an aza-, an oxa-, or a thiabicyclo[3.1.0]hex-6-yl ring system were synthesized, and their in vitro antibacterial activity and structure-activity relationships (SAR) were evaluated. Most of the synthesized
