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N-(E)-[2-(phenylamino)cyclopent-1-en-1-yl]methylideneaniline is a complex organic chemical compound that is a derivative of aniline. It features an additional cyclopentene ring and a phenylamino group attached to the carbon-carbon double bond, which contributes to its high aromaticity. N-(E)-[2-(phenylamino)cyclopent-1-en-1-yl]methylideneaniline is of interest in the fields of organic synthesis and pharmaceutical research due to its unique structural features and potential reactivity. It is crucial to handle this chemical with care, as it may have health risks if not managed with proper safety measures.

30159-83-2

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30159-83-2 Usage

Uses

Used in Organic Synthesis:
N-(E)-[2-(phenylamino)cyclopent-1-en-1-yl]methylideneaniline is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for multiple points of reactivity, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N-(E)-[2-(phenylamino)cyclopent-1-en-1-yl]methylideneaniline is used as a starting material or intermediate in the development of new drugs. Its aromatic and reactive nature may contribute to the discovery of novel therapeutic agents with unique mechanisms of action.
Used in Chemical Research:
N-(E)-[2-(phenylamino)cyclopent-1-en-1-yl]methylideneaniline is utilized in academic and industrial research settings to study the properties of complex organic molecules. Its reactivity and structural features make it an interesting subject for investigations into reaction mechanisms, molecular interactions, and the development of new synthetic methodologies.
Used in Material Science:
In material science, N-(E)-[2-(phenylamino)cyclopent-1-en-1-yl]methylideneaniline may be employed in the development of new materials with specific properties, such as high thermal stability, unique optical characteristics, or specific binding affinities. Its aromatic system and potential for molecular modification make it a candidate for creating advanced materials with tailored properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 30159-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,5 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30159-83:
(7*3)+(6*0)+(5*1)+(4*5)+(3*9)+(2*8)+(1*3)=92
92 % 10 = 2
So 30159-83-2 is a valid CAS Registry Number.

30159-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(phenyliminomethyl)cyclopenten-1-yl]aniline

1.2 Other means of identification

Product number -
Other names Benzenamine,N-[[2-(phenylamino)-1-cyclopenten-1-yl]methylene]-,monohydrochloride (9CI)

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:30159-83-2 SDS

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