1200-16-4

Basic information

• Product Name: Benzene, 1-chloro-4-[(methoxymethoxy)methyl]-
• CAS NO: 1200-16-4
• Molecular Formula: C9H11ClO2
• Molecular Weight: 186.638
• Mol File: 1200-16-4.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-4-[(methoxymethoxy)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-4-[(methoxymethoxy)methyl]-(1200-16-4)
• EPA Substance Registry System: Benzene, 1-chloro-4-[(methoxymethoxy)methyl]-(1200-16-4)

Safety Data

• Hazardous Substances Data: 1200-16-4(Hazardous Substances Data)

Upstream product

• 109-87-5 Dimethoxymethane 
• 873-76-7 para-Chlorobenzyl alcohol 
• 106-48-9 4-chloro-phenol 
• 107-30-2 chloromethyl methyl ether 
• 29540-84-9 4-chlorophenyl trifluoromethanesulfonate 

Downstream Products

• 207223-84-5 {4-[(methoxymethoxy)methyl]phenyl}methanol 
• 98-85-1 1-Phenylethanol 
• 873-76-7 para-Chlorobenzyl alcohol 
• 100-51-6 benzyl alcohol 
• 140-53-4 p-chlorobenzyl cyanide 
• 35424-56-7 1-chloro-4-(iodomethyl)benzene 
• 622-95-7 4-chlorobenzyl bromide 
• 1195776-98-7 C₉H₁₀⁽²⁾HClO₂ 
• 1195776-99-8 (4-chlorophenyl)methoxymethoxymethyltrimethylsilane 
• 5406-33-7 4-chlorobenzyl acetate 
• 14856-74-7 4-chlorobenzyltrimethylsilyl ether 

Relevant articles and documents

Catalytic application of sulfamic acid-functionalized magnetic Fe3O4nanoparticles (SA-MNPs) for protection of aromatic carbonyl compounds and alcohols: Experimental and theoretical studies

Protection techniques of functional groups within the structure of organic compounds are important synthetic methods against unwanted attacks from various reagents during synthetic sequences. Acetal and thioacetal groups are well known as protective funct

Palladium-catalyzed direct hydroxymethylation of aryl halides and triflates with potassium acetoxymethyltrifluoroborate

Suzuki-Miyaura cross-coupling reactions of aryl halides and triflates with potassium acetoxymethyltrifluoroborate afforded the corresponding aryl and heteroaryl methanol products in moderate to excellent yields.

[InCl4]: An efficient catalyst-medium for alkoxymethylation of alcohols and their interconversion to acetates and TMS-ethers

A simple, green and chemoselective method for methoxymethylation and ethoxymethylation of primary and secondary alcohols using a Lewis acidic room temperature ionic liquid, [C4mim][InCl4], as catalyst and reaction medium under ambient temperature, microwave and ultrasonic irradiations is reported. In this catalytic system, the corresponding MOM-and EOM-ethers are obtained in excellent yields and in short reaction times. Furthermore, this catalytic system was used for mild and efficient transformations of these protected alcohols to their corresponding acetates and trimethylsilyl ethers under thermal conditions and microwave and ultrasonic irradiations.