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2-(o-aminophenyl)-5-methylthiophe is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96919-46-9

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96919-46-9 Usage

Structure

2-(o-aminophenyl)-5-methylthiophene is a thiophene derivative with an amino group (-NH2) and a methyl group (-CH3) attached to the thiophene ring.

Aromatic properties

The compound is known for its aromatic characteristics, which contribute to its stability and reactivity in chemical reactions.

Building block in organic synthesis

It is commonly used as a building block to create a variety of functionalized thiophene derivatives.

Potential applications

2-(o-aminophenyl)-5-methylthiophene has been studied for its potential use in materials science, organic electronics, and pharmaceuticals.

Development of dyes, polymers, and other organic compounds

Due to its aromatic properties, the compound has been utilized in the development of various organic compounds, including dyes and polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 96919-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,9,1 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96919-46:
(7*9)+(6*6)+(5*9)+(4*1)+(3*9)+(2*4)+(1*6)=189
189 % 10 = 9
So 96919-46-9 is a valid CAS Registry Number.

96919-46-9Downstream Products

96919-46-9Relevant academic research and scientific papers

2-(anilinomethyl)imidazolines as alpha1A adrenergic receptor agonists: 2'-heteroaryl and 2'-oxime ether series.

Navas 3rd., Frank,Bishop, Michael J,Garrison, Deanna T,Hodson, Stephen J,Speake, Jason D,Bigham, Eric C,Drewry, David H,Saussy, David L,Liacos, James H,Irving, Paul E,Gobel, M Jeffrey

, p. 575 - 579 (2007/10/03)

A series of 2'-heteroaryl and 2'-oxime anilinomethylimidazolines was prepared and evaluated in in vitro functional assays for cloned human alpha1A, alpha1B, and alpha1D receptor subtypes. Potent and selective alpha1A agonists have been identified in these series.

INTRAMOLECULAR DIAZO COUPLING OF 2-AMINOPHENYLTHIOPHENES. THE FORMATION OF ISOMERIC THIENOCINNOLINES

Barton, John W.,Lapham, David J.,Rowe, David J.

, p. 131 - 134 (2007/10/02)

Thieno- (4) and thieno-cinnolines (7) have been obtained by diazotisation and internal coupling of the corresponding 2-(o-aminophenyl)thiophenes.By the same reaction 3-(o-aminophenyl)-2,5-dimethylthiophene gives 1,3-dimethylthienolcinnoline (9).

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