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2972-73-8

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2972-73-8 Usage

Description

(3-chlorobenzylidene)propanedinitrile, with the molecular formula C11H7ClN2, is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. It is a chemical compound known for its versatile chemical properties and potential applications across various fields.

Uses

Used in Pharmaceutical Industry:
(3-chlorobenzylidene)propanedinitrile is used as a chemical intermediate for the production of various pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of drugs with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, (3-chlorobenzylidene)propanedinitrile serves as a chemical intermediate, contributing to the development of compounds used in agriculture for pest control and crop protection.
Used in Organic Synthesis:
(3-chlorobenzylidene)propanedinitrile is utilized as a reagent in organic synthesis, facilitating the creation of a wide range of organic compounds for various applications.
Used in Materials Science:
Its potential use in materials science stems from the compound's ability to contribute to the development of new materials with specific properties, such as those with enhanced stability or reactivity.
Used as a Precursor for Aromatic Compounds:
(3-chlorobenzylidene)propanedinitrile also acts as a precursor for the synthesis of other aromatic compounds, which are important in various chemical and industrial processes.
It is crucial to handle and use (3-chlorobenzylidene)propanedinitrile with care due to its potential toxic or harmful effects if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 2972-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2972-73:
(6*2)+(5*9)+(4*7)+(3*2)+(2*7)+(1*3)=108
108 % 10 = 8
So 2972-73-8 is a valid CAS Registry Number.

2972-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(3-chlorophenyl)methylidene]propanedinitrile

1.2 Other means of identification

Product number -
Other names m-chlorobenzylidene malononitrile

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:2972-73-8 SDS

2972-73-8Relevant articles and documents

Reversible Phase Transfer of Carbon Dots between an Organic Phase and Aqueous Solution Triggered by CO2

Pei, Xiaoyan,Xiong, Dazhen,Wang, Huiyong,Gao, Shuaiqi,Zhang, Xinying,Zhang, Suojiang,Wang, Jianji

, p. 3687 - 3691 (2018)

Carbon dots (CDs) have attracted increasing attention in applications such as bio-imaging, sensors, catalysis, and drug delivery. However, unlike metallic and semiconductor nanoparticles, the transfer of CDs between polar and non-polar phases is little un

First organocatalytic asymmetric synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives

Auria-Luna, Fernando,Marqués-López, Eugenia,Herrera, Raquel P.

, (2018)

Preliminary results concerning the first asymmetric synthesis of highly functionalized 1-benzamido-1,4-dihydropyridine derivatives via the reaction of hydrazones with alkylidenemalononitriles in the presence of β-isocupreidine catalyst are reported. The m

Effect of supramolecular polymeric aggregation in room temperature ionic liquids (RTILs) on catalytic activity in the synthesis of 4H-chromene derivatives and Knoevenagel condensation

Muhammad, Shoaib,Ali, Firdous Imran,Javed, Muhammad Naveed,Wasim, Agha Arsalan,Bari, Ahmed,Rafique, Faisal,Ilyas, Muhammad Amjad,Riaz, Kashif,Mahmood, Syed Junaid,Ahmed, Amir,Hashmi, Imran Ali

, (2020/10/30)

RTILs exhibit supramolecular self-assembled polymeric aggregation due to noncovalent interactions. The influence of the aggregation behaviour of RTILs on catalytic activity is evident but still poorly understood. The present work focuses on establishing a

Development of an efficient, one-pot, multicomponent protocol for synthesis of 8-hydroxy-4-phenyl-1,2-dihydroquinoline derivatives

Tabassum, Rukhsana,Ashfaq, Muhammad,Oku, Hiroyuki

, p. 534 - 547 (2020/12/04)

A one-pot quick and efficient multicomponent reaction has been developed for the synthesis of a new series of functionalized 8-hydroxy-4-phenyl-1,2-dihydroquinoline derivatives using 30 mol% ammonium acetate in ethanol as solvent. This economical protocol

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