73406-52-7

Basic information

• Product Name: 2-O-methoxymethylbenzyl bromide
• Synonyms: 2-O-methoxymethylbenzyl bromide
• CAS NO: 73406-52-7
• Molecular Weight: 231.089
• Mol File: 73406-52-7.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2-O-methoxymethylbenzyl bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O-methoxymethylbenzyl bromide(73406-52-7)
• EPA Substance Registry System: 2-O-methoxymethylbenzyl bromide(73406-52-7)

Safety Data

• Hazardous Substances Data: 73406-52-7(Hazardous Substances Data)

Upstream product

• 5533-04-0 2-(methoxymethoxy)benzaldehyde 
• 27701-23-1 methyl 2-(methoxymethyloxy)benzoate 
• 119-36-8 methyl salicylate 
• 69-72-7 salicylic acid 
• 90-02-8 salicylaldehyde 
• 89-95-2 2-methyl-benzyl alcohol 
• 95-48-7 ortho-cresol 
• 55359-65-4 1-methoxymethoxy-2-methylbenzene 
• 73406-54-9 (2-Methoxymethoxyphenyl)methyl-methansulfonat 
• 5533-05-1 (2-methoxymethoxyphenyl)methanol 

Downstream Products

• 152955-18-5 methyl 2-(4-methoxyphenyl)-3-(2-O-methoxymethylphenyl)propanoate 
• 152955-17-4 methyl 2-(2-methoxyphenyl)-3-(2-O-methoxymethylphenyl)propanoate 
• 169125-15-9 (+)-(4S,5R)-1,5-dimethyl-4-phenyl-3-<2'-(4-methoxyphenyl)-3'-(2-O-methoxymethylphenyl)>propionyl-2-imidazolidinone 
• 169125-26-2 (-)-(4R,5S)-1,5-dimethyl-4-phenyl-3-<2'-(4-methoxyphenyl)-3'-(2-O-methoxymethylphenyl)>propionyl-2-imidazolidinone 
• 58732-18-6 o-[4-hydroxy-3-methyl-2(Z)-butenyl]phenol 
• 110983-49-8 (E)-2-methoxymethoxy-4'-acetoxystilbene 
• 110983-47-6 (E)-2-methoxymethoxy-4'-dimethylaminostilbene 

Relevant articles and documents

Regioselective Fluorination of Acenes: Tailoring of Molecular Electronic Levels and Solid-State Properties

Optoelectronic properties of molecular solids are important for organic electronic devices and are largely determined by the adopted molecular packing motifs. In this study, we analyzed such structure-property relationships for the partially regioselectiv

Hydrogen-atom abstraction/cyclization in synthesis. Direct syntheses of coumestan and coumestrol

The synthesis of coumestrol has been achieved in five steps from 1,3-dimethoxybenzene. The key step is a photochemical cyclization of a glyoxylate ester.

The direct synthesis of isoflavans VIA α-alkylation of phenylacetates

Deprotonation of oxygenated phenylacetates and quenching of the enolates with oxygenated benzylic electrophiles, afforded 2,3-diarylpropanoates which served as precursors to the isoflavans following consecutive reduction and cyclization steps.