6765-75-9 Usage
Molecular Structure
1H-Indole structure with a carboxaldehyde group and a 5-chloro-3-phenyl substituent.
Usage
Often used as an intermediate in the synthesis of various pharmaceutical products and organic compounds.
Industry Applications
Potential applications in the pharmaceutical industry due to its ability to form important chemical bonds and functional groups.
Biological Activities
May have biological activities and potential therapeutic properties.
Research Interest
Of interest for further research and development in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 6765-75-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,6 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6765-75:
(6*6)+(5*7)+(4*6)+(3*5)+(2*7)+(1*5)=129
129 % 10 = 9
So 6765-75-9 is a valid CAS Registry Number.
6765-75-9Relevant academic research and scientific papers
Metal-free synthesis of 1H-indole-2-carbaldehydes by N-iodosuccinimide- mediated cyclization of 1-(2′-anilinyl)prop-2-yn-1-ols in water. A formal synthesis of (R)-calindol
Kothandaraman, Prasath,Lauw, Sherman Jun Liang,Chan, Philip Wai Hong
, p. 7471 - 7480 (2013/08/23)
A N-iodosuccinimide (NIS)-mediated method to prepare 1H-indole-2- carbaldehydes efficiently from cycloisomerization of 1-(2-aminophenyl)prop-2-yn- 1-ols is described. The reaction is operationally straightforward and accomplished in good to excellent yiel
Synthesis of Substituted 7H-INdoloisoquinolines
Hiremath, Shiva Yogi P.,Badami, Prema S.,Purohit, Muralidhar G.
, p. 1235 - 1238 (2007/10/02)
Various substituted ethyl 3-phenylindole-2-carbamates (4a-f) have been synthesised through the intermediacy of carboxyhydrazides (2a-f) and carboxyazides (3a-f) and converted into 5,6-dihydro-7H-indoloisoquinolin-5(6H)-ones (5a-f) by refluxing in d
