569337-39-9 Usage
Uses
Used in Pharmaceutical Industry:
5-(Benzyloxy)-3-bromo-1H-indole is used as a building block for the synthesis of various pharmaceuticals. Its unique chemical reactivity allows for the development of new drugs with potential therapeutic applications.
Used in Organic Chemistry Research:
5-(benzyloxy)-3-bromo-1H-indole is also utilized in organic chemistry research to explore its reactivity and potential use in the synthesis of other organic compounds. Its presence in the development of new chemical reactions and methodologies contributes to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 569337-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,9,3,3 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 569337-39:
(8*5)+(7*6)+(6*9)+(5*3)+(4*3)+(3*7)+(2*3)+(1*9)=199
199 % 10 = 9
So 569337-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H12BrNO/c16-14-9-17-15-7-6-12(8-13(14)15)18-10-11-4-2-1-3-5-11/h1-9,17H,10H2
569337-39-9Relevant academic research and scientific papers
Synthesis and biological activities of isogranulatimide analogues
Hugon, Bernadette,Anizon, Fabrice,Bailly, Christian,Golsteyn, Roy M.,Pierre, Alain,Leonce, Stephane,Hickman, John,Pfeiffer, Bruno,Prudhomme, Michelle
, p. 5965 - 5980 (2008/03/15)
The synthesis of new isogranulatimide analogues, their inhibitory activities toward the Checkpoint 1 kinase (Chk1), and their in vitro cytotoxicities toward four tumor cell lines (one murine L1210 leukemia, and three human cell lines: DU145 prostate carci
Synthesis of isogranulatimide analogues possessing a pyrrole moiety instead of an imidazole heterocycle
Hugon, Bernadette,Pfeiffer, Bruno,Renard, Pierre,Prudhomme, Michelle
, p. 3927 - 3930 (2007/10/03)
An efficient four step synthesis from commercial indoles of isogranulatimide analogues is reported. In the new compounds, the imidazole moiety is replaced by a pyrrole unit, the indole part is substituted or not in 5-position and the nitrogen of the imide moiety bears or not a methyl substituent.
