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2-(3,4-diaminoanilino)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72584-60-2

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72584-60-2 Usage

Amino alcohol

Structure classification
2-(3,4-diaminoanilino)ethanol is classified as an amino alcohol due to the presence of both amino groups and a hydroxyl group in its structure.

Benzene ring

Core structure
The compound has a benzene ring as its core structure, which is a stable six-membered ring with alternating single and double bonds between carbon atoms.

Amino groups

Two amino groups (-NH2)
The compound contains two amino groups attached to the benzene ring at the 3rd and 4th positions, which contribute to its reactivity and biological activity.

Ethyl group

Attached to hydroxyl substituent (-CH2CH3)
An ethyl group (-CH2CH3) is attached to a hydroxyl group (-OH) in the structure, further enhancing its reactivity and potential applications.

Pharmaceutical applications

Production of pharmaceuticals
2-(3,4-diaminoanilino)ethanol is commonly used in the production of various pharmaceuticals due to its unique structure and reactivity.

Dyes and polymers

Production of dyes and polymers
The compound is also used in the production of dyes and polymers, showcasing its versatility in different industries.

Building block for organic synthesis

Organic synthesis applications
2-(3,4-diaminoanilino)ethanol serves as a building block for organic synthesis, allowing for the creation of more complex molecules and compounds.

Reagent in chemical reactions

Use as a reagent
The compound is used as a reagent in various chemical reactions, further demonstrating its utility in the field of chemistry.

Biological activities and therapeutic effects

Potential for research and development
2-(3,4-diaminoanilino)ethanol has potential biological activities and may exhibit therapeutic effects, making it an important compound for research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 72584-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,8 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72584-60:
(7*7)+(6*2)+(5*5)+(4*8)+(3*4)+(2*6)+(1*0)=142
142 % 10 = 2
So 72584-60-2 is a valid CAS Registry Number.

72584-60-2Relevant academic research and scientific papers

DERIVATIVES OF 5(6)-AMINOBENZIMIDAZOLE CONTAINING STERICALLY HINDERED PHENOLIC GROUPS

Sokolova, N. Yu.,Kuznetsov, V. A.,Garabadzhiu, A. V.,Sokolov, V. V.,Ginak, A. I.

, p. 544 - 549 (2007/10/02)

By the condensation of 2-methoxyethyl carboximidate hydrochlorides with o-diamines we obtained 5(6)-aminobenzimidazole derivatives containing sterically hindered phenolic groups at C2 of the imidazole ring.On the basis of UV-spectral data it was shown tha

DERIVATIVES OF 5(6)-AMINOBENZIMIDAZOLE

Kuznetsov, V. A.,Garabadzhiu, A. V.,Ginzburg, O. F.

, p. 576 - 580 (2007/10/02)

A series of triamines were obtained by the amination of 2-nitro-5-chloroaminobenzene and reduction of the obtained compounds.In reaction with the esters of aromatic acids the products were converted into derivatives of 5(6)-aminobenzimidazole.

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