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Carbamic acid, (5-chloro-3-phenyl-1H-indol-2-yl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70070-39-2

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70070-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70070-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,7 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70070-39:
(7*7)+(6*0)+(5*0)+(4*7)+(3*0)+(2*3)+(1*9)=92
92 % 10 = 2
So 70070-39-2 is a valid CAS Registry Number.

70070-39-2Relevant academic research and scientific papers

Synthesis of Substituted 1,2,3,8-Tetrahydroindolobenzodiazepin-2-ones and 5,6,7,8-Tetrahydroindolobenzodiazepin-6-ones

Hiremath, Shivayogi P.,Badami, Prema S.,Purohit, Muralidhar G.

, p. 1115 - 1119 (2007/10/02)

Nitrosation (NaNO2/AcOH) of 2-phenylindoles (1a-d) and subsequent reduction of the resultant 3-nitroso-2-phenylindoles (2a-d) with sodium dithionite in alkali furnish the corresponding 3-aminoindoles (3a-d), which on condensation with ethyl chloroformate

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

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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