91714-50-0 Usage
General Description
7-(4-Bromobenzoyl)indole, also known as 4-Bromobenzoylindole or 7-bromo-1H-indol-3-yl)phenyl)methanone, is a chemical compound with the molecular formula C18H12BrNO. It belongs to the class of organic compounds known as indoles and derivatives, which are compounds containing an indole ring, which is a bicyclic 2,3-benzopyrrole, and an indole derivative carrying a benzoyl group. 7-(4-Bromobenzoyl)indole is commonly used in the field of organic synthesis and pharmaceutical research. 7-(4-Bromobenzoyl)indole has several potential applications in the fields of medicinal chemistry and drug discovery due to its ability to modulate various biological pathways and targets. It may be used as a starting material for the synthesis of other pharmaceutical compounds or as a research tool for studying the mechanisms of action of certain drugs. Additionally, it has been implicated in some studies as a potential therapeutic agent for the treatment of various diseases and conditions, although further research is needed to fully understand its pharmacological properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 91714-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,1 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91714-50:
(7*9)+(6*1)+(5*7)+(4*1)+(3*4)+(2*5)+(1*0)=130
130 % 10 = 0
So 91714-50-0 is a valid CAS Registry Number.
91714-50-0Relevant articles and documents
Antifungal and/or antiparasitic pharmaceutical composition and novel indole derivatives as active principle of such a composition
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Page/Page column 20, (2010/02/06)
The present invention relates to novel indole derivatives, their method of preparation and their pharmacological activity as antimycotic and/or antiparasitic compounds.
Process for the production of 7-acylindoles
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, (2008/06/13)
A process for the production of 7-acylindoles of the general formula: STR1 starting from indoline of the formula: STR2 Indoline is cyanized in a first stage to 7-cyanoindoline of the formula: STR3 The latter is catalytically dehydrogenated in a second stage to 7-cyanindole of the formula: STR4 The latter is then acylated in a third stage with an organometallic compound of the formula: into the end product according to formula I.