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1-(naphthalen-2-yl)ethan-1-amine hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39110-76-4

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39110-76-4 Usage

Salt form

1-(naphthalen-2-yl)ethan-1-amine

Usage

Intermediate in the synthesis of various pharmaceuticals and organic compounds

Physical appearance

White to off-white crystalline solid

Solubility

Soluble in water and ethanol

Melting point

Around 238-239°C

Potential application

Serotonin receptor agonist

Therapeutic potential

Treatment of disorders such as depression and anxiety

Safety precautions

Handle and use with care due to potential risks to human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 39110-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,1 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39110-76:
(7*3)+(6*9)+(5*1)+(4*1)+(3*0)+(2*7)+(1*6)=104
104 % 10 = 4
So 39110-76-4 is a valid CAS Registry Number.

39110-76-4Upstream product

39110-76-4Downstream Products

39110-76-4Relevant academic research and scientific papers

Resolution of alpha-(phenoxy) phenylacetic acid derivatives with naphthyl-alkylamines

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Page/Page column 10, (2008/06/13)

The present invention provides a methods and compounds for producing an enantiomerically enriched α-(phenoxy)phenylacetic acid compound of the formula: from a mixture of its enantiomers, where R1 is alkyl or haloalkyl and X is halide.

Selective Conversion of Benzylic C-H Bonds to an Amine Function by Oxidative Nucleophilic Substitution

Guy, Alain,Lemor, Alain,Doussot, Joel,Lemaire, Marc

, p. 900 - 902 (2007/10/02)

The benzylic proton of alkylarenes 1 was replaced by an azido group in one step by reaction with trimethylsilyl azide or hydrazoic acid in chloroform in the presence of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ).The 1-arylalkyl azides 2 were reduced to amines 3, which were characterized as their hydrochlorides 4.

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