826-26-6

Basic information

• Product Name: Benzene, 1-chloro-4-(methoxymethoxy)-
• Synonyms: Methyl-p-chlorphenyl-formal;4-Chlor-methoxymethoxybenzol;1-methoxymethoxy-4-chlorobenzene;(4-Chlor-phenoxy)-methoxy-methan
• CAS NO: 826-26-6
• Molecular Formula: C8H9ClO2
• Molecular Weight: 172.611
• Mol File: 826-26-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-4-(methoxymethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-4-(methoxymethoxy)-(826-26-6)
• EPA Substance Registry System: Benzene, 1-chloro-4-(methoxymethoxy)-(826-26-6)

Safety Data

• Hazardous Substances Data: 826-26-6(Hazardous Substances Data)

Upstream product

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

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 
• 51985-33-2 5-Chloro-2-methoxymethoxy-benzoic acid 
• 106-48-9 4-chloro-phenol 
• 115560-50-4 3-(5-Chloro-2-methoxymethoxy-phenyl)-3-hydroxy-N,N-dimethyl-propionamide 
• 321-14-2 5-chloro-2-hydroxybenzoic acid 
• 89488-25-5 (5‐chloro‐2‐hydroxyphenyl)boronic acid 
• 947683-03-6 C₇H₇ClCH₂O₂BHO₂C₆H₁₀ 

Relevant articles and documents

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.

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 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