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1H-Indole-2-carboxamide,N-(2-aminophenyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

497825-38-4

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497825-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497825-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,8,2 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 497825-38:
(8*4)+(7*9)+(6*7)+(5*8)+(4*2)+(3*5)+(2*3)+(1*8)=214
214 % 10 = 4
So 497825-38-4 is a valid CAS Registry Number.

497825-38-4Downstream Products

497825-38-4Relevant academic research and scientific papers

An anion receptor that facilitates transmembrane proton-anion symport by deprotonating its sulfonamide N-H proton

Shinde, Sopan Valiba,Talukdar, Pinaki

, p. 10351 - 10354 (2018)

Indole-based amide-sulfonamide derivatives were synthesized. The X-ray crystal structure and chloride binding studies in solution showed a 1?:?1 stoichiometry. The ion transport efficiency directly correlated to the pKa of the sulfonamide N-H p

N-monoacylated derivatives of o-phenylenediamines, their analogs and their use as pharmaceutical agents

-

, (2008/06/13)

New compounds represented by the formula or pharmaceutically acceptable salts or prodrugs thereof, wherein X1 and X2 are each independently selected from a CH group or a nitrogen atom; and R is an optionally substituted five or six membered nonaromatic carbocyclic ring or a nonaromatic or aromatic heterocyclic ring, whereby the ring is optionally condensed with a 6-membered, optionally substituted carbocyclic aromatic ring.

SYNTHESIS OF 1H-INDOLYL-2-BENZIMIDAZOLES AND 1H-INDOLYL-2-BENZOTHIAZOLES

Hudkins, Robert L.

, p. 1045 - 1050 (2007/10/02)

A convenient synthesis of regioisomeric 1H-indolyl-2-benzimidazoles and -2-benzothiazoles by the direct conversion of indoleesters with the in situ generated organoaluminum reagents trimethylaluminum-1,2-diaminobenzene or trimethylaluminum-2-aminothiophenol is reported.

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