392717-83-8

Basic information

• Product Name: Benzene, 1-[(methoxymethoxy)methyl]-4-(phenylmethoxy)-
• CAS NO: 392717-83-8
• Molecular Formula: C16H18O3
• Molecular Weight: 258.317
• Mol File: 392717-83-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1-[(methoxymethoxy)methyl]-4-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-[(methoxymethoxy)methyl]-4-(phenylmethoxy)-(392717-83-8)
• EPA Substance Registry System: Benzene, 1-[(methoxymethoxy)methyl]-4-(phenylmethoxy)-(392717-83-8)

Safety Data

• Hazardous Substances Data: 392717-83-8(Hazardous Substances Data)

Upstream product

• 836-43-1 4-benzyloxybenzyl alcohol 
• 107-30-2 chloromethyl methyl ether 
• 109-87-5 Dimethoxymethane 

Downstream Products

• 836-43-1 4-benzyloxybenzyl alcohol 
• 1015081-06-7 C₉H₁₂O₃ 
• 113195-57-6 1-iodomethyl-4-benzyloxybenzene 
• 5544-60-5 4-(benzyloxy)benzyl bromide 
• 838-96-0 2-[4-(benzyloxy)phenyl]acetonitrile 
• 624286-53-9 (4-(benzyloxy)benzyloxy)trimethylsilane 
• 59184-20-2 2-bromo-(trimethylsilyloxymethyl)benzene 
• 82466-12-4 2-bromobenzyl acetate 

Relevant articles and documents

NON-LINEAR SELF-IMMOLATIVE LINKERS AND CONJUGATES THEREOF

The present invention relates to linker-drug compounds (LDs) and antibody-drug conjugates (ADCs) comprising a non-linear self-immolative linker, which is cleavable or transformable under appropriate conditions and which reduces the hydrophobicity of the a

[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.