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(3-Fluoro-4-nitrophenyl)methanamine hydrochloride is a chemical compound that features a substituted aniline ring with a fluoro and a nitro group attached to it, along with a methanamine functional group. This hydrochloride salt form is widely utilized in organic synthesis and medicinal chemistry, and is recognized for its potential in the development of pharmaceuticals and agrochemicals due to its diverse biological activities. Additionally, it serves as a building block in the synthesis of various organic compounds and may have applications in materials science and catalysis.

199486-37-8

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199486-37-8 Usage

Uses

Used in Pharmaceutical Development:
(3-Fluoro-4-nitrophenyl)methanamine hydrochloride is used as a key intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs with diverse therapeutic profiles.
Used in Agrochemical Synthesis:
In the agrochemical industry, (3-Fluoro-4-nitrophenyl)methanamine hydrochloride is used as a precursor in the creation of agrochemicals, aiming to enhance crop protection and yield through the development of novel compounds with specific pesticidal properties.
Used in Organic Synthesis:
(3-Fluoro-4-nitrophenyl)methanamine hydrochloride is utilized as a building block in organic synthesis, allowing for the construction of a variety of complex organic molecules for research and commercial applications.
Used in Materials Science:
(3-Fluoro-4-nitrophenyl)methanamine hydrochloride is explored in the field of materials science for its potential to contribute to the development of new materials with unique properties, such as improved stability or reactivity.
Used in Catalysis:
(3-Fluoro-4-nitrophenyl)methanamine hydrochloride may be employed as a catalyst or in the development of catalytic systems to enhance the efficiency of chemical reactions in various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 199486-37-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,4,8 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 199486-37:
(8*1)+(7*9)+(6*9)+(5*4)+(4*8)+(3*6)+(2*3)+(1*7)=208
208 % 10 = 8
So 199486-37-8 is a valid CAS Registry Number.

199486-37-8Downstream Products

199486-37-8Relevant academic research and scientific papers

The first synthesis of 16+15-membered bicyclic polypeptide model of A- O-C-B-O-D rings of kistamicin

Beugelmans, Rene,Gonzalez Zamora, Eduardo,Roussi, Georges

, p. 8189 - 8192 (1997)

A 16+15 membered bicyclic polypeptide containing biaryl ether bonds, model of A-O-C-B-O-D rings of kistamicin has been synthesized by sequential intramolecular SN(Ar) reactions.

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