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4-Amino-3,4-dihydro-2H-naphthalen-1-one, also known as 4-Amino-1-tetralone, is an organic compound with the molecular formula C10H11NO. It is a derivative of naphthalene, featuring a naphthalene ring with an amino group at the 4th position and a carbonyl group at the 1st position. 4-Amino-3,4-dihydro-2H-naphthalen-1-one is recognized for its potential as a significant building block in the production of various biologically active compounds. Its versatile reactivity and potential for biological activity contribute to its wide range of applications in the pharmaceutical and chemical industries.

61895-10-1

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61895-10-1 Usage

Uses

Used in Pharmaceutical Industry:
4-Amino-3,4-dihydro-2H-naphthalen-1-one is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of biologically active compounds. Its presence in the molecular structure of these compounds can enhance their therapeutic effects and pharmacological properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Amino-3,4-dihydro-2H-naphthalen-1-one is utilized as an intermediate in the synthesis of agrochemicals, where it plays a role in creating compounds that can be used in pest control and crop protection. Its chemical properties allow for the development of effective and targeted agrochemical products.
Used in Chemical Synthesis:
4-Amino-3,4-dihydro-2H-naphthalen-1-one is employed as a key building block in the chemical synthesis of a variety of organic compounds. Its unique structure and reactivity make it a valuable component in the creation of complex molecules for various applications, including but not limited to, materials science, dyes, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 61895-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,9 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61895-10:
(7*6)+(6*1)+(5*8)+(4*9)+(3*5)+(2*1)+(1*0)=141
141 % 10 = 1
So 61895-10-1 is a valid CAS Registry Number.

61895-10-1Relevant academic research and scientific papers

Novel mast cell-stabilising amine derivatives of 3,4-dihydronaphthalen- 1(2H)-one and 6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-one

Barlow, James W.,Zhang, Tao,Woods, Orla,Byrne, Adam J.,Walsh, John J.

, p. 213 - 223 (2012/05/20)

In an investigation of 4-amino-3,4-dihydronaphthalen-1(2H)-ones as novel modulators of allergic and inflammatory phenomena, we have investigated a series of cyclic analogues. Tertiary amines of structural types 9, 10, 20 and 21 were synthesised and evaluated for mast cell stabilising activity. In vitro and in vivo studies showed that of these compounds, the cyclohexenylamino derivatives of tetralone and benzosuberone of series 20 and 21 exhibited interesting activity both in vitro and in vivo.

Direct Photoamination of Arenes with Ammonia and Primary Amines in the Presence of Electron Acceptors

Yasuda, Masahide,Yamashita, Toshiaki,Shima, Kensuke,Pac, Chyongjin

, p. 753 - 759 (2007/10/02)

Direct photoamination of phenanthrene, 9-methoxyphenanthrene, anthracene, naphthalene, and several substituted naphthalenes with ammonia or primary amines in the presence of m-dicyanobenzene occurs to give aminated dihydroarenes in fairly good yields. m-Dimethoxybenzene and biphenyl are photoaminated in lower yields.A suggested mechanism for the photoamination involves the nucleophilic attack of ammonia and amines on aromatic cation radicals generated by photochemical electron transfer to m-dicyanobenzene.The present photoamination is applied to direct introduction of various functionalized primary amines containing the vinyl, cyano, hydroxy, acetylamino, and ethoxycarbonyl groups.

Synthesis of 1,2,3,4-tetrahydro-4-oxo-[or oxy-]-1-naphthylureas as novel growth-promoting compounds for animals

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, (2008/06/13)

This invention relates to novel 1,2,3,4-tetrahydro-4-oxo-[-oxy-]-1-naphthylurea compounds and their derivatives. This invention also relates to method for the preparation of said compounds. This invention further relates to methods for the use of said tetrahydro-4-oxo-[oxy-]-1-naphthylurea compounds as animal growth regulators.

Novel 1,2,3,4-tetrahydro-4-oxo-(oxy)-1-naphthylamines and method of preparation thereof

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, (2008/06/13)

This disclosure describes 1,2,3,4-tetrahydro-4-oxo-(oxy)-1-naphthylamine and novel derivatives thereof and methods of preparation of said compounds. These novel compounds are useful and valuable intermediates for the preparation of 1,2,3,4-tetrahydro-4-oxo(oxy)-1-naphthylurea and thiourea compounds and certain derivatives thereof which are animal growth promoters.

1-Benzoyl-3-(1,2,3,4-tetrahydro-4-oxo-1-naphthyl)-urea, a novel and useful intermediate for the preparation of animal growth promoting agents

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, (2008/06/13)

This invention relates to 1-benzoyl (and 1-substituted benzoyl)-3-(1,2,3,4-tetrahydro-4-oxo-1-naphthyl)ureas, novel and useful intermediates for the preparation of 1,2,3,4-tetrahydro-4-oxo-1-naphthylurea and certain derivatives thereof. The above tetrahydro-4-oxo-1-naphthyl-urea and certain derivatives thereof are animal growth promoting agents. This invention further relates to methods of preparation of said 1-benzoyl (and 1-substituted benzoyl) 3-(1,2,3,4-tetrahydro-4-oxo-1-naphthyl)ureas.

Tetrahydro-4-imino-1-naphthylureas

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, (2008/06/13)

There are provided certain substituted-1,2,3,4-tetrahydro-4-imino-1-naphthylureas, methods of preparation thereof, and methods of use of said naphthylureas for enhancing feed efficiency and for promoting the growth rate of veterinary homothermic animals.

Hydroxycitric acid derivatives

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, (2008/06/13)

Ester and amide derivatives of three-hydroxycitric acid γ-lactone inhibit fatty acid synthesis in biological systems and are useful in the treatment of obesity and in correcting conditions of lipid abnormalities.

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