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104245-83-2

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104245-83-2 Usage

Description

5-(chloroethyl)-2-methyltoluene, also known as 3,4-Dimethyl-1-(1-chloroethyl)benzene, is an organic compound characterized by the presence of a chloroethyl group attached to a methyltoluene moiety. This unique structure endows it with specific chemical properties that make it a valuable reagent in various applications.

Uses

Used in Pharmaceutical Industry:
5-(chloroethyl)-2-methyltoluene is used as an organic reagent for the synthesis of phenylethyl derivatives in pharmaceutical applications. Its specific chemical structure allows for targeted drug development, particularly in the creation of compounds that can interact with biological systems in a controlled manner.
The reason for its use in pharmaceutical synthesis is due to its ability to serve as a building block for the development of new drugs, especially those that require a phenylethyl framework. This makes it a versatile component in the design and synthesis of a wide range of pharmaceutical agents, potentially leading to innovative treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 104245-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,4 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104245-83:
(8*1)+(7*0)+(6*4)+(5*2)+(4*4)+(3*5)+(2*8)+(1*3)=92
92 % 10 = 2
So 104245-83-2 is a valid CAS Registry Number.

104245-83-2Upstream product

104245-83-2Downstream Products

104245-83-2Relevant articles and documents

Process for the preparation of substituted vinylbenzyl chloride

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, (2008/06/13)

An improved continous single step vapor phase process for the preparation of substituted vinylbenzyl chloride from substituted ethyltoluene is disclosed. In this process a substituted ethyltoluene is reacted with a halogen gas in the vapor phase, at elevated temperatures via a continuous feed process. Furthermore, this process achieves halogenation followed by dehydrohalogenation in a single pass through the reactor. There is also obtained a very high total selectivity to vinylbenzyl chloride and its precursors via this continuous process.

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