27441-79-8

Basic information

• Product Name: Benzene, 1,1'-[(2-methylene-1,3-propanediyl)bis(oxymethylene)]bis-
• CAS NO: 27441-79-8
• Molecular Formula: C18H20O2
• Molecular Weight: 268.356
• Mol File: 27441-79-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[(2-methylene-1,3-propanediyl)bis(oxymethylene)]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[(2-methylene-1,3-propanediyl)bis(oxymethylene)]bis-(27441-79-8)
• EPA Substance Registry System: Benzene, 1,1'-[(2-methylene-1,3-propanediyl)bis(oxymethylene)]bis-(27441-79-8)

Safety Data

• Hazardous Substances Data: 27441-79-8(Hazardous Substances Data)

Upstream product

• 1871-57-4 2-chloromethyl-3-chloroprop-1-ene 
• 100-51-6 benzyl alcohol 
• 3513-81-3 2-(Hydroxymethyl)allyl alcohol 
• 100-39-0 benzyl bromide 

Downstream Products

• 145215-00-5 ethyl 1,1-bis(benzyloxymethyl)cyclopropane-2-carboxylate 
• 77356-14-0 1,3-dibenzyloxy-2-propanone 
• 774587-66-5 1-(2-benzyloxymethylallyl)cyclohexanecarboxaldehyde 
• 1058138-87-6 1-benzyl-4-methylene-2-pentylpyrrolidine 
• 1332646-37-3 C₂₃H₂₈O₄ 
• 1397441-82-5 1-isocyano-2,2-bis[2',2'-di(benzyloxymethyl)ethoxymethyl]ethane 
• 1380599-06-3 1-amino-2,2-bis[2',2'-di(benzyloxymethyl)ethoxymethyl]ethane 
• 1380599-05-2 1-azido-2,2-bis[2',2'-di(benzyloxymethyl)ethoxymethyl]ethane 
• 1380599-04-1 2,2-bis[2',2'-di(benzyloxymethyl)ethoxymethyl]ethane mesylate 
• 778592-64-6 2,2-bis[2',2'-di(benzyloxymethyl)ethyoxymethyl]ethanol 
• 1380598-98-0 2,2-bis[2',2'-di(benzyloxymethyl)ethoxymethyl]ethene 
• 145215-24-3 6-<<2,2-bis(benzyloxymethyl)cyclopropyl>amino>-4-chloro-2,5-diformamidopyrimidine 
• 145215-26-5 N-[9-(2,2-Bis-benzyloxymethyl-cyclopropyl)-6-chloro-9H-purin-2-yl]-formamide 
• 145215-29-8 9-<2,2-bis(benzyloxymethyl)cyclopropyl>guanine 

Relevant articles and documents

Convergent synthesis of dendrimers via the passerini three-component reaction

Tuning properties by programming the surface functional group composition of surface-block dendrimers has been limited to dendrimers with only two types of surface functionality (i.e., surface-diblock dendrimers). The Passerini reaction provides dendrimer

Convenient synthesis of pyrrolidines by amphiphilic allylation of imines with 2-methylenepropane-1,3-diols

(Chemical Equation Presented). A straightforward route: The combination of a palladium catalyst and triethylborane promotes the amphiphilic (nucleophilic-electrophilic) allylation of aldimines, prepared in situ from a wide variety of aromatic and aliphatic aldehydes and amines, with commercially available 2-methylenepropane-1,3-diols to provide pyrrolidines (see scheme).

Studies of intramolecular alkylidene carbene reactions; an approach to heterocyclic nucleoside bases

A series of investigations into the applications of intramolecular cyclisations of alkylidene carbenes are described. The insertion reaction of the carbene generated from 1,4-di(tert-butyldimethylsilyloxy)-3-benzyloxy-butane-2-one to the benzylic position