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1-amino-9b-(4-methylphenyl)-1,4,5,9b-tetrahydro-2H-azeto[2,1-a]isoquinolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62333-79-3

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62333-79-3 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 20 carbon (C) atoms, 21 hydrogen (H) atoms, 3 nitrogen (N) atoms, and 1 oxygen (O) atom.
2. Azetoisoquinoline Derivative

Explanation

1-Amino-9b-(4-methylphenyl)-1,4,5,9b-tetrahydro-2H-azeto[2,1-a]isoquinolin-2-one belongs to the azetoisoquinoline class, which is a group of chemical compounds known for their diverse biological activities.

Explanation

The presence of an amino group (-NH2) and a tetrahydroazeto ring system (a six-membered ring with two carbonyl groups and four hydrogen atoms) in the molecule contribute to its potential pharmaceutical applications.
4. Potential Pharmaceutical Applications

Explanation

Due to its structural features, 1-Amino-9b-(4-methylphenyl)-1,4,5,9b-tetrahydro-2H-azeto[2,1-a]isoquinolin-2-one may have potential applications in the pharmaceutical industry, although further research is needed to fully understand its properties and potential uses.

Explanation

The isoquinoline-based structure of 1-Amino-9b-(4-methylphenyl)-1,4,5,9b-tetrahydro-2H-azeto[2,1-a]isoquinolin-2-one suggests that it may have biological effects, particularly on the central nervous system. However, more research is required to confirm these effects and determine the compound's specific mechanisms of action.

Explanation

While 1-Amino-9b-(4-methylphenyl)-1,4,5,9b-tetrahydro-2H-azeto[2,1-a]isoquinolin-2-one shows promise due to its structural features and potential biological effects, additional research is necessary to fully comprehend its properties, potential applications, and any possible side effects or limitations.

Structural Features

Amino group and tetrahydroazeto ring system

Biological Effects

Possible activity on the central nervous system

Further Research

Required to understand properties and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 62333-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,3 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62333-79:
(7*6)+(6*2)+(5*3)+(4*3)+(3*3)+(2*7)+(1*9)=113
113 % 10 = 3
So 62333-79-3 is a valid CAS Registry Number.

62333-79-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-9b-(4-methylphenyl)-4,5-dihydro-1H-azeto[2,1-a]isoquinolin-2-one

1.2 Other means of identification

Product number -
Other names 1-Amino-9b-(4-methylphenyl)-1,4,5,9b-tetrahydro-2H-azeto(2,1-a)isoquinolin-2-one

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:62333-79-3 SDS

62333-79-3Downstream Products

62333-79-3Relevant academic research and scientific papers

Some Novel Monocyclic cis-β-Lactams from Glycine

Sharma, S. D.,Gupta, P. K.

, p. 760 - 764 (2007/10/02)

Enamine derivatives (Ia, b) obtained by the condensation of glycine and β-dicarbonyl compounds have been utilised for the stereoselective synthesis of cis-β-lactams.Addition of POCl3 to a mixture of the potassium salts (I), imines (IIa-c and III) and triethylamine gives 3-enamino-2-azetidinones (IV, VI, VII, X and XXI) in 30-40 percent yield.Imines (IId and IIe) prepared from ethyl glycinate hydrochloride and aromatic aldehydes, when subjected to this reaction yield 3-enamino-β-lactams (XIII and XVII) carrying an ester function.The protecting β-dicarbonyl function canbe easily removed with ethanol/HCl to generate the α-amino-β-lactams (V, VIII, XI, XIV, XVIII and XXII) which have been used as the progenitors for the preparation of 3-amido-2-azetidinones.The α-amido-β-lactams (XV and XIX) having an ester function on treatment with 0.1 N NaOH in acetone get converted into the novel α-amido-β-lactams (XVI and XX) carrying a free carboxy function essential for antibacterial activity.

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