84522-35-0 Usage
Description
3-[(2,2-dimethoxyethyl)thio]propene is a colorless liquid chemical compound with the molecular formula C7H14O2S. It features a propene backbone with a thioether functional group and two dimethoxyethyl substituents, making it a versatile building block in organic synthesis for various chemical reactions.
Uses
Used in Pharmaceutical Industry:
3-[(2,2-dimethoxyethyl)thio]propene is used as a key intermediate in the synthesis of pharmaceuticals for its ability to react with other compounds to form a variety of products, contributing to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical field, 3-[(2,2-dimethoxyethyl)thio]propene is utilized as a precursor in the production of agrochemicals, playing a crucial role in the synthesis of compounds that help protect crops and enhance agricultural productivity.
Used in Materials Science:
3-[(2,2-dimethoxyethyl)thio]propene is employed as a component in materials science applications, where its unique chemical structure allows for the creation of new materials with specific properties for various uses, such as in coatings, adhesives, or polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 84522-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,2 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84522-35:
(7*8)+(6*4)+(5*5)+(4*2)+(3*2)+(2*3)+(1*5)=130
130 % 10 = 0
So 84522-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2S/c1-4-5-10-6-7(8-2)9-3/h4,7H,1,5-6H2,2-3H3
84522-35-0Relevant articles and documents
Processes for making 3-methylthiophene-2-carboxaldehyde and intermediates therefor
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, (2008/06/13)
Processes for preparing isomerically pure 3-methylthiophene-2-carboxaldehyde, an intermediate for synthesis of anthelmintic agents, by reaction of mercaptoacetaldehyde or the dimer, or a polymer thereof, or a dialkylacetal thereof in the presence of a base with (1) methyl vinyl ketone or an alpha- or beta-oxidized derivative of methyl vinyl ketone to form a 3-oxobutylmercaptoacetaldehyde or dialkyl acetal thereof, or an alpha- or beta-substituted derivative thereof which is then converted to 3-methylthiophene-2-carboxaldehyde via appropriate steps including, if necessary, treatment with acid, followed, if necessary, by enamine catalyzed cyclization and, in the case of using methyl vinyl ketone as reactant, a dehydrogenation step; or (2) 3-butyn-2-one to produce a mixture of isomeric 3-oxobut-1-enylmercaptoacetaldehyde or dialkyl acetals thereof which is cyclized to 3-methylthiophene-2-carboxaldehyde. A further aspect of this invention is an improved process for making dialkyl acetals of 2-mercaptoacetaldehyde which comprises reacting an alkyl vinyl ether with sulfur chloride to produce a bis(2-chloro-2-alkoxy ethyl)disulfide which is then treated with an alcohol to afford a bis(2,2-dialkoxyethyl)disulfide which is reduced under alkaline conditions to 2-mercaptoethyl acetaldehyde alkali metal salt which can be alkylated to a thioether, a valuable intermediate.
