71056-60-5 Usage
Uses
Used in Pharmaceutical Industry:
1H-Indole-2-carboxylic acid, 6-amino-, ethyl ester (9CI) is used as a building block for the synthesis of various pharmaceutical drugs. Its unique structure and functional groups make it a valuable component in the development of new therapeutic agents.
Used in Antibacterial Applications:
1H-Indole-2-carboxylicacid,6-amino-,ethylester(9CI) is utilized as an antibacterial agent, targeting a range of bacterial pathogens. Its ability to inhibit bacterial growth and disrupt essential cellular processes makes it a promising candidate for the development of new antibiotics.
Used in Antifungal Applications:
1H-Indole-2-carboxylic acid, 6-amino-, ethyl ester (9CI) is employed as an antifungal agent, effective against various fungal species. Its potential to interfere with fungal cell wall synthesis and other vital functions contributes to its antifungal activity.
Used in Anticancer Applications:
This chemical is used as an anticancer agent, exhibiting potential to inhibit the growth and proliferation of cancer cells. Its ability to target specific molecular pathways and disrupt cancer cell survival mechanisms makes it a valuable compound in the search for novel cancer therapies.
Used in Drug Development Research:
1H-Indole-2-carboxylic acid, 6-amino-, ethyl ester (9CI) is used as a research tool in drug development, aiding scientists in understanding the mechanisms of action and potential applications of indole-based compounds. Its versatility and reactivity in chemical reactions facilitate the exploration of new drug candidates and therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 71056-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,5 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71056-60:
(7*7)+(6*1)+(5*0)+(4*5)+(3*6)+(2*6)+(1*0)=105
105 % 10 = 5
So 71056-60-5 is a valid CAS Registry Number.
71056-60-5Relevant academic research and scientific papers
Methods for dyeing keratinous fibres with aminoindoles, compositions and devices for use
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, (2008/06/13)
Method for dyeing keratinous fibres, in particular human keratinous fibres, such as hair, characterized in that a composition (A) containing, in a medium appropriate for dyeing, at least one aminoindole corresponding to the formula: STR1 in which: R1 and R3, independently of one another, represent a hydrogen atom or a C1 -C4 alkyl group; R2 denotes hydrogen or a C1 -C4 alkyl group or COOR', R' being a hydrogen atom or a C1 -C4 alkyl group; R4 represents a hydrogen atom or a C1 -C4 alkyl, C1 -C4 hydroxyalkyl or C2 -C4 polyhydroxyalkyl group; Z1 represents a hydrogen or halogen atom or a C1 -C4 alkyl group or OR; R being a hydrogen atom or a C1 -C4 alkyl group; and Z2 represents a hydrogen atom or a C1 -C4 alkyl group; and its salts is applied to said fibres, the colour being developed with the aid of an oxidizing system.
Synthesis of Isomeric Benzodipyrroles
Katti, H. A.,Siddappa, S.
, p. 1205 - 1208 (2007/10/02)
Ethyl aminoindole-2-carboxylates (2), obtained by catalytic reduction of ethyl nitroindole-2-carboxylates (1) using Raney nickel, when subjected to Japp-Klingemann reaction furnish the respective indolylhydrazones (3).The latter undergo cyclization with H2SO4 to yield different isomeric benzodipyrroles (4-6).
