935285-60-2 Usage
Uses
Used in Organic Synthesis:
Tert-butyl (5-bromo-2-fluorophenyl)carbamate is used as a protecting group for amines due to its ability to be easily added and removed under mild conditions, facilitating the synthesis of complex organic molecules.
Used in Medicinal Chemistry and Pharmaceutical Research:
In the field of medicinal chemistry, tert-butyl (5-bromo-2-fluorophenyl)carbamate is utilized for the development of potential drug candidates. Its unique structural features make it a valuable component in the design and synthesis of new pharmaceuticals.
Used in Chemical Research:
Tert-butyl (5-bromo-2-fluorophenyl)carbamate is also employed in chemical research to study the reactivity and properties of carbamate derivatives, contributing to the understanding of their behavior in various chemical reactions.
Safety Note:
It is crucial to handle tert-butyl (5-bromo-2-fluorophenyl)carbamate with care, as it may possess toxic or harmful effects if not used properly. Adequate safety measures should be taken to minimize any potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 935285-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,2,8 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 935285-60:
(8*9)+(7*3)+(6*5)+(5*2)+(4*8)+(3*5)+(2*6)+(1*0)=192
192 % 10 = 2
So 935285-60-2 is a valid CAS Registry Number.
935285-60-2Relevant academic research and scientific papers
Design, synthesis, and pharmacological evaluation of N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives as potent glycogen phosphorylase inhibitors
Onda, Kenichi,Shiraki, Ryota,Ogiyama, Takashi,Yokoyama, Kazuhiro,Momose, Kazuhiro,Katayama, Naoko,Orita, Masaya,Yamaguchi, Tomohiko,Furutani, Masako,Hamada, Noritaka,Takeuchi, Makoto,Okada, Minoru,Ohta, Mitsuaki,Tsukamoto, Shin-ichi
experimental part, p. 10001 - 10012 (2009/04/06)
As a result of the various N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives with a hydroxy moiety synthesized in an effort to discover novel glycogen phosphorylase (GP) inhibitors, 5-chloro-N-(5-hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)-1H-indole-2
