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N-[4-(1-Amino-ethyl)-phenyl]-acetamide hydrochloride is a chemical compound characterized by an acetamide group linked to a phenyl ring, with an additional aminoethyl group attached. It is commonly encountered as a hydrochloride salt, which enhances its stability and solubility. N-[4-(1-Amino-ethyl)-phenyl]-acetamide hydrochloride holds promise in chemical and pharmaceutical research, particularly for the development of novel drugs and biologically active molecules. Its structural features suggest potential interactions with biological receptors and enzymes, positioning it as a valuable asset for investigating molecular dynamics within living systems.

120342-71-4

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120342-71-4 Usage

Uses

Used in Chemical Research:
N-[4-(1-Amino-ethyl)-phenyl]-acetamide hydrochloride is utilized as a research compound for exploring its chemical properties and potential reactivity with other molecules. Its unique structure allows scientists to study its interactions and possible applications in various chemical processes.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N-[4-(1-Amino-ethyl)-phenyl]-acetamide hydrochloride serves as a key component in the development of new drugs. Its ability to potentially interact with biological receptors and enzymes makes it a candidate for designing drugs targeting specific diseases or conditions.
Used in Drug Design and Development:
N-[4-(1-Amino-ethyl)-phenyl]-acetamide hydrochloride is employed as a building block in the design of new pharmaceuticals. Its structural attributes may contribute to the creation of drugs with enhanced efficacy and selectivity, improving treatment outcomes for various medical conditions.
Used in Biological Studies:
N-[4-(1-Amino-ethyl)-phenyl]-acetamide hydrochloride is also used as a tool in biological research to investigate molecular interactions within living organisms. Its potential to engage with receptors and enzymes provides insights into biological processes and mechanisms, aiding in the understanding of disease pathways and the development of targeted therapies.
Used in Industrial Processes:
The hydrochloride salt form of N-[4-(1-Amino-ethyl)-phenyl]-acetamide hydrochloride offers improved stability and solubility, making it suitable for use in various industrial applications. Its properties can be harnessed to enhance the efficiency and effectiveness of chemical reactions and processes in different sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 120342-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,4 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 120342-71:
(8*1)+(7*2)+(6*0)+(5*3)+(4*4)+(3*2)+(2*7)+(1*1)=74
74 % 10 = 4
So 120342-71-4 is a valid CAS Registry Number.

120342-71-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-(1-aminoethyl)phenyl)acetamide hydrochloride

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:120342-71-4 SDS

120342-71-4Downstream Products

120342-71-4Relevant academic research and scientific papers

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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