59579-08-7

Basic information

• Product Name: Benzene, 1-chloro-2-(methoxymethyl)-
• CAS NO: 59579-08-7
• Molecular Formula: C8H9ClO
• Molecular Weight: 156.612
• Mol File: 59579-08-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-2-(methoxymethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-2-(methoxymethyl)-(59579-08-7)
• EPA Substance Registry System: Benzene, 1-chloro-2-(methoxymethyl)-(59579-08-7)

Safety Data

• Hazardous Substances Data: 59579-08-7(Hazardous Substances Data)

Upstream product

• 124-41-4 sodium methylate 
• 611-17-6 1-bromomethyl-2-chlorobenzene 
• 611-19-8 1-chloro-2-(chloromethyl)benzene 
• 7803-57-8 hydrazine hydrate 
• 89-98-5 2-chloro-benzaldehyde 
• 149-73-5 trimethyl orthoformate 
• 617-86-7 triethylsilane 
• 610-96-8 methyl chlorobenzoate 
• 17849-38-6 2-Chlorobenzyl alcohol 
• 74-88-4 methyl iodide 
• 13057-19-7 Iodomethyl methyl ether 
• 148651-35-8 2-chlorophenylzinc iodide 
• 694-80-4 2-bromo-1-chlorobenzene 
• 27490-32-0 tributyl(methoxymethyl)stannane 

Downstream Products

• 610-96-8 methyl chlorobenzoate 
• 6269-46-1 2-(2-chlorophenyl)-1,3-benzothiazole 
• 185896-88-2 ethyl 2-(2-methoxymethyl-phenyl)-2-oxoacetate 
• 89-98-5 2-chloro-benzaldehyde 

Relevant articles and documents

A Versatile Iridium(III) Metallacycle Catalyst for the Effective Hydrosilylation of Carbonyl and Carboxylic Acid Derivatives

A versatile iridium(III) metallacycle catalysed rapidly and selectively the reduction of a large array of challenging esters and carboxylic acids as well as various ketones and aldehydes. The reactions proceeded in high yields at room temperature by hydrosilylation followed by desilylation. Although the reactions of various aldehydes and ketones resulted exclusively in alcohols, the hydrosilylation of esters led to alcohols or ethers, depending on the type of substrate. Regarding the carboxylic acids, again the nature of the reagent controlled the outcome of the hydrosilylation reaction, either alcohols or aldehydes being formed.

Ferric perchlorate as an efficient and useful catalyst for the selective benzylation and methylation of alcohols with benzyl chloride and methyl iodide

A mild and efficient method was developed for selective benzylation and methylation of hydroxyl compounds in the presence of a catalytic amount of ferric perchlorate. We showed that ferric perchlorate was very effective in selectively promoting the benzylation and methylation of primary aliphatic and benzylic alcohols versus secondary aliphatic alcohols and phenolic hydroxy groups. Graphical abstract: [Figure not available: see fulltext.]

PROCESS FOR PRODUCING N-METHYL-METHOXYIMINOACETAMIDE DERIVATIVES AND INTERMEDIATES THEREOF

A method for producing an N-methyl-methoxyiminoacetamide derivative represented by the following general formula (I) (wherein R3represents a hydrogen atom or a group represented by a general formula -C(R4)(R5)-Ar (wherein