135710-38-2

Usage

Uses

Used in Organic Chemistry:
METHYL 3,5-BIS(ALLYLOXY)BENZENECARBOXYLATE is used as a reagent in organic chemistry for [application reason]. It aids in the synthesis of various organic compounds, contributing to the advancement of chemical research and development.
Used in Pharmaceutical Production:
In the pharmaceutical industry, METHYL 3,5-BIS(ALLYLOXY)BENZENECARBOXYLATE is used as an intermediate for [application reason]. Its role in the production process is vital for creating a range of pharmaceuticals that address various health conditions.
Used in Chemical Product Manufacturing:
METHYL 3,5-BIS(ALLYLOXY)BENZENECARBOXYLATE is used as an important intermediate in the manufacturing of various chemical products for [application reason]. Its presence in the production process ensures the creation of diverse chemical products that serve different industries and applications.

InChI:InChI=1/C14H16O4/c1-4-6-17-12-8-11(14(15)16-3)9-13(10-12)18-7-5-2/h4-5,8-10H,1-2,6-7H2,3H3

Upstream product

• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 106-95-6 allyl bromide 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 67-56-1 methanol 

Downstream Products

• 139954-63-5 methyl 2,6-diallyl-3,5-dihydroxybenzoate 
• 139954-64-6 methyl 2,4-diallyl-3,5-dihydroxybenzoate 
• 177837-80-8 3,5-bis(prop-2-en-1-yloxy)benzyl alcohol 
• 185254-52-8 3,5-bis(allyloxy)benzoic acid 
• 749870-73-3 3,5-bis(4-oxobutoxy)benzoic acid methyl ester 
• 1000773-37-4 3,5-bis(allyloxy)benzoic acid chloride 
• 1318617-11-6 N,N'-bis[[1-(3,5-diglycidoxyphenyl)-1-methylethoxy]carbonyl]toluene-2,4-diamine 
• 1318617-08-1 N,N'-bis[[1-(3,5-diglycidoxyphenyl)-1-methylethoxy]carbonyl]hexane-1,6-diamine 
• 1318617-06-9 N,N'-bis[[1-(3,5-hydroxyphenyl)-1-methylethoxy]-carbonyl]toluene-2,4-diamine 
• 1318617-03-6 N,N'-bis[[1-(3,5-dihydroxyphenyl)-1-methylethoxy]carbonyl]hexane-1,6-diamine 
• 1318616-99-7 N,N'-bis[[1-(3,5-diallyloxyphenyl)-1-methylethoxy]carbonyl]toluene-2,4-diamine 
• 1318616-97-5 N,N'-bis[[1-(3,5-diallyloxyphenyl)-1-methylethoxy]carbonyl]hexane-1,6-diamine 
• 1318616-95-3 1-(3,5-diallyloxyphenyl)-1-methylethanol 
• 182058-69-1 3,5-diallyoxyphenylmethylbromide 

Relevant academic research and scientific papers

Green synthesis of (R)-terbutaline for recyclable catalytic asymmetric transfer hydrogenation in ionic liquids

We synthesize optically active (R)-terbutaline 2, which is an anti-asthmatic drug, through recyclable catalytic asymmetric transfer hydrogenation (RCATH). Various chloroketones 4 were prepared and RCATH was performed on them. The products exhibit moderate

High-Boron-Content Porphyrin-Cored Aryl Ether Dendrimers: Controlled Synthesis, Characterization, and Photophysical Properties

The synthesis and characterization of a set of poly(aryl ether) dendrimers with tetraphenylporphyrin as the core and 4, 8, 16, or 32 closo-carborane clusters are described. A regioselective hydrosilylation reaction on the allyl-terminated functions with c

Thermally activated, single component epoxy systems

A single component epoxy system in which the resin and hardener components found in many two-component epoxies are combined onto the same molecule is described. The single molecule precursor to the epoxy resin contains both multiple epoxide moieties and a

Fabrication of self-assembled dendron monolayers

A dendron (2) comprising a focal point (4) and a plurality of fluorinated end groups (9) is disclosed, including one having a thiol, a silane, a carboxylic acid, a phosphonate or another moiety at the focal point suitable for chemisorption to a substrate

Synthesis of supercritical carbon dioxide soluble perfluorinated dendrons for surface modification

(Chemical Equation Presented) The rational design, synthesis, and characterization of a series of novel perfluorinated dendrons 14a,b, 25a,b, 26a,b, and 18 are described. The dendrimers were designed to have a thiol at the focal point for attachment to a gold surface to enable the fabrication of self-assembled monolayers (SAMs). Perfluorinated tails were attached to the periphery to provide solubility in supercritical carbon dioxide, and to increase the hydrophobicity and the stability of self-assembled monolayers formed. Mitsunobu reactions were utilized to provide high-yielding steps allowing large-scale production of the novel dendrimers.

Incorporation of functional guest molecules into an internally functionalizable dendrimer through olefin metathesis

A poly(aryl ether) dendrimer bearing 22 allyl groups throughout the interior of the molecule has been prepared using a convergent synthetic approach. The internal functionalities of this dendrimer can be used to attach small molecule guests to the interio

Helical porous protein mimics self-assembled from amphiphilic dendritic dipeptides

This manuscript reports the synthesis and the self-assembly of (4-3,4,5-3,5)nG2-CH2-Boc-L-Tyr-L-Ala-OMe dendritic dipeptides (n = 12, 16). These dendritic dipeptides self-assemble both in solution and in solid states into helical por

Cross-linking dendrimers with allyl ether end-groups using the ring-closing metathesis reaction

A third generation Frechet-type dendrimer containing 24 allyl ether end-groups was synthesized, cross-linked using the ring-closing metathesis (RCM) reaction, and the core was removed hydrolytically without significant fragmentation. The results are analo

Rapid synthesis of dendrimers based on calix[4]resorcinarenes

Calix[4]resorcinarenes are phenolic macrocyclic compounds, and readily available from resorcinols and aldehydes. We were interested in calix[4]resorcinarenes as highly functionalized core molecules for the rapid synthesis of dendrimers because of their ea

Induction of liquid crystallinity by host-guest interactions

A molecular clip is described which binds aromatic guests by an induced fit mechanism. It contains twelve long aliphatic chains and can evoke liquid-crystalline properties in a variety of molecules, including polymers and porphyrins, by a process of molecular recognition.