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5-methyl-indole-2-carboxylic acid hydrazide is an organic compound with the chemical formula C10H10N2O2. It is a derivative of indole-2-carboxylic acid, featuring a methyl group at the 5th position and a hydrazide group attached to the carboxylic acid. 5-methyl-indole-2-carboxylic acid hydrazide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain alkaloids and other biologically active molecules. Its structure allows for further chemical modifications, making it a valuable building block in organic synthesis.

1463-64-5

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1463-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1463-64-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1463-64:
(6*1)+(5*4)+(4*6)+(3*3)+(2*6)+(1*4)=75
75 % 10 = 5
So 1463-64-5 is a valid CAS Registry Number.

1463-64-5Relevant academic research and scientific papers

NEW TRIAZINOINDOLE COMPOUNDS

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Page/Page column 60-61, (2021/11/06)

The invention relates to novel compounds for use as inhibitors of NLRP3 inflammasone production, wherein such compounds are as defined by compounds of formula (I) and wherein the integers R1, R2, R3a and R3b are defined in the description, and where the compounds may be useful as medicaments, for instance for use in the treatment of a disease or disorder that is associated with NLRP3 inflammasome activity.

Synthesis of Substituted 2-(1',3',4'-Oxadiazol-2'-yl)indoles

Sinnur, K. H.,Siddappa, S.,Hiremath, Shivayogi P.,Purohit, Muralidhar G.

, p. 716 - 720 (2007/10/02)

Substituted indole-2-carboxylic acid hydrazides (2) on refluxing with ethyl orthoformate give the respective 2-(1',3',4'-oxadiazol-2'-yl)indoles (4).These compounds have also been obtained by reacting 2 with formamide to get the corresponding N-formyl der

Synthesis of Substituted 2-(5'-Oxo/thioxo-1',3',4'-oxodiazol-2'-yl)indoles and 2-(5'-Oxo/thioxo-1,3,4'-oxodiazol-2'-ylamino)indoles

Hiremath, Shivayogi P.,Hiremath, Dakshayani M.,Purohit, Muralidhar G.

, p. 571 - 576 (2007/10/02)

Indole-2-carboxylates (1a-i) and indole-2-carbamates (12d-i) react with hydrazine hydrate in ethanol to give the corresponding hydrazides (2a-i) and semicarbazides (13d-i).These compounds when heated under reflux with CS2 and KOH give 2-(5'-thioxo-1',3',4'-oxadiazol-2'-yl)indoles (5c,g) and 2-(5'-thioxo-1',3',4'-oxadiazol-2'-ylamino)indoles (16f,g,i).Compounds 2a-i and 13d-i undergo condensation with ethyl chloroformate to give the products 3a-g and 14d,g,h, respectively which on heating under reflux with diphenyl ether give the corresponding 2-(5'-oxo-1',3',4'-oxadiazol-2'-yl)indoles (4a-g) and 2-(5'-oxo-1',3',4'-oxadiazol-2'-ylimino)indoles (15d,g,h).Ethyl 2-phenylindole-3-carbamate (18), obtained from 3-aminoindole (17), has been condensed with hydrazine hydrate to give the semicarbazide (19) which on reation with ethyl chloroformate and heating under reflux with diphenyl ether produces 3-(5'-oxo-1',3',4'-oxadiazol-2'-ylamino)indole (21).

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