13533-31-8 Usage
Description
4-chloro-N-[(E)-thiophen-2-ylmethylidene]aniline is a chemical compound with the molecular formula C11H8ClNS. It is a yellow to light brown solid that is classified as an aniline derivative, containing a chloro group and a thiophen-2-ylmethylidene group. 4-chloro-N-[(E)-thiophen-2-ylmethylidene]aniline is used in the synthesis of various organic compounds and has potential applications in the pharmaceutical and agricultural industries.
Uses
Used in Pharmaceutical Industry:
4-chloro-N-[(E)-thiophen-2-ylmethylidene]aniline is used as a building block for the synthesis of various biologically active compounds. Its unique chemical structure allows it to be incorporated into the development of new drugs with potential therapeutic benefits.
Used in Agricultural Industry:
In the agricultural industry, 4-chloro-N-[(E)-thiophen-2-ylmethylidene]aniline is used as a building block for the synthesis of various agrochemicals. Its potential applications include the development of new pesticides, herbicides, and other crop protection agents.
Used as a Dye:
4-chloro-N-[(E)-thiophen-2-ylmethylidene]aniline has been studied for its potential applications as a dye due to its yellow to light brown color. It can be used in various industries that require coloration, such as textiles, plastics, and printing inks.
Used as an Indicator:
4-chloro-N-[(E)-thiophen-2-ylmethylidene]aniline has also been studied for its potential use as an indicator in various chemical reactions. Its unique chemical properties may allow it to change color or exhibit other visual changes in response to specific conditions, making it useful for monitoring reactions or detecting the presence of certain substances.
Used as a Corrosion Inhibitor:
4-chloro-N-[(E)-thiophen-2-ylmethylidene]aniline has been investigated for its potential as a corrosion inhibitor. Its chemical structure may provide protective properties against corrosion in various materials, making it useful in industries such as metal processing, construction, and automotive.
However, it is important to handle 4-chloro-N-[(E)-thiophen-2-ylmethylidene]aniline with care, as it can be harmful if inhaled, swallowed, or absorbed through the skin, and can cause irritation to the respiratory system and skin. Proper safety measures should be taken during its use and handling to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 13533-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13533-31:
(7*1)+(6*3)+(5*5)+(4*3)+(3*3)+(2*3)+(1*1)=78
78 % 10 = 8
So 13533-31-8 is a valid CAS Registry Number.
13533-31-8Relevant articles and documents
Synthesis of Green/Blue Light Emitting Quinolines by Aza-D-A Reaction Using InCl3 Catalyst
Singh, Rajkumar Romeshkumar,Singh, Thokchom Prasanta,Singh, Ningthoujam Premananda,Naorem, Shanta Singh,Singh, Okram Mukherjee
, p. 247 - 257 (2020/11/24)
An efficient InCl3-catalyzed sequential reaction of aromatic amines, aromatic aldehydes and functionalized alkynes leading to the formation of new quinoline derivatives exhibiting significant fluorescence activities is described. The photophysi
Heterogeneous Catalysis with Basic Compounds to Achieve the Synthesis and C-N Cleavage of Azetidin-2-ones under Microwave Irradiation
Alcaraz, Yolanda,Cruz, Francisco,De La Cruz, Fabiola N.,Delgado, Francisco,Domínguez, José Manuel,Galván, Adriana,Gomez, Clarisa Villegas,Martínez, Merced,Vázquez, Miguel A.
supporting information, p. 3625 - 3637 (2019/09/30)
The synthesis of azetidin-2-ones with a completely heterogeneous catalysis is reported. The use of basic compounds as solid catalysts allowed for the synthesis of azetidin-2-ones under microwave irradiation without organic additives such as triethylamine. An excellent catalyst for this transformation was Mg-Al hydroxide (MAH). The present methodology offers the advantages of non-hazardous reaction conditions, short reaction times, high yields, and catalyst reusability. Different substitution groups were tested on the imines and acyl chlorides to explore the scope of the reaction. Unconventional N-C4 bond cleavage was detected in azetidin-2-ones. MAH was characterized by N 2 adsorption-desorption, X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HR-TEM).
A simple method for the synthesis of 1,3-diaminopropan-2-ols derivatives and their ex vivo relaxant activity on isolated rat tracheal rings
López, Fabiola I.,de la Cruz, Fabiola N.,López, Julio,Martínez, J. Merced,Alcaraz, Yolanda,Delgado, Francisco,Sánchez-Recillas, Amanda,Estrada-Soto, Samuel,Vázquez, Miguel A.
, p. 1325 - 1335 (2017/05/04)
Abstract: A mild and eco-friendly method has been developed for the synthesis of a series of 1,3-diaminopropan-2-ols 8a–n. The epoxide of epichlorohydrin undergoes ring-opening with amines using MgSO4 or mixed metal oxides catalysts under mild