826-26-6

Upstream product

• 107-30-2 chloromethyl methyl ether 
• 106-48-9 4-chloro-phenol 
• 109-87-5 Dimethoxymethane 

Downstream Products

• 115560-38-8 2-(methoxymethoxy)-5-chlorobenzaldehyde 
• 271601-01-5 4-bromo-2-[5-chloro-2-(methoxymethoxy)phenyl]thiazole 
• 609352-56-9 2-methoxymethoxy-5-chlorophenylboronic acid 
• 106-48-9 4-chloro-phenol 
• 89488-25-5 (5‐chloro‐2‐hydroxyphenyl)boronic acid 
• 115560-50-4 3-(5-Chloro-2-methoxymethoxy-phenyl)-3-hydroxy-N,N-dimethyl-propionamide 
• 321-14-2 5-chloro-2-hydroxybenzoic acid 
• 947683-03-6 C₇H₇ClCH₂O₂BHO₂C₆H₁₀ 
• 51985-33-2 5-Chloro-2-methoxymethoxy-benzoic acid 

Relevant academic research and scientific papers

P4VPy–CuO nanoparticles as a novel and reusable catalyst: application at the protection of alcohols, phenols and amines

P4VPy–CuO nanoparticles were synthesized using ultrasound irradiations. Relevant properties of the synthesized nanoparticles were investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Fourier transform infrared spectroscopy. After identification, the prepared reagent was used for the promotion of different types of protection reactions of alcohols, phenols and amines. Easy workup, short reaction times, excellent yields, relatively low cost and reusability of the catalyst are the striking features of the reported methods.

Siladifluoromethylation and Difluoromethylation onto C(sp3), C(sp2), and C(sp) Centers Using Ruppert-Prakash Reagent and Fluoroform

Siladifluoromethylations and difluoromethylations on sp3, sp2, and sp carbons of lithiated carbamates, arenes, and terminal alkynes, respectively, have been attained by employing the Ruppert-Prakash reagent (CF3TMS) and fl

Enantiodivergent Atroposelective Synthesis of Chiral Biaryls by Asymmetric Transfer Hydrogenation: Chiral Phosphoric Acid Catalyzed Dynamic Kinetic Resolution

Reported herein is an enantiodivergent synthesis of chiral biaryls by a chiral phosphoric acid catalyzed asymmetric transfer hydrogenation reaction. Upon treatment of biaryl lactols with aromatic amines and a Hantzsch ester in the presence of chiral phosp

Highly efficient and selective methoxymethylation of alcohols and phenols catalyzed by reusable ZrO(OTf)2 under solvent-free conditions

Different primary, secondary, and tertiary alcohols were efficiently converted to their corresponding methoxymethyl ethers with formaldehyde dimethyl acetal in the presence of catalytic amounts of ZrO(OTf)2 at room temperature. Phenols were als

Highly efficient and selective methoxymethylation of alcohols and phenols catalyzed by high-valent tin(IV) porphyrin

An efficient and selective method for methoxymethylation of alcohols and phenols with formaldehyde dimethyl acetal (FDMA) catalyzed by electron deficient tin(IV)tetraphenylporphyrinato trifluoromethanesulfonate, [SnIV(TPP)(OTf)2], is

High-valent [SnIV(Br8TPP)(OTf)2] as a highly efficient and reusable catalyst for selective methoxymethylation of alcohols and phenols: The effect of substituted bromines on the catalytic activity

High-valent tin(IV)octabromotetraphenylporphyrinato trifluoromethanesulfonate, [SnIV(Br8TPP)(OTf)2], was used for selective methoxymethylation of alcohols and phenols with formaldehyde dimethyl acetal (FDMA) at room temper