185254-52-8

Basic information

• Product Name: 3,5-BIS(ALLYLOXY)BENZENECARBOXYLIC ACID
• Synonyms: 3,5-BIS(ALLYLOXY)BENZENECARBOXYLIC ACID
• CAS NO: 185254-52-8
• Molecular Formula: C₁₃H₁₄O₄
• Molecular Weight: 234.25
• Mol File: 185254-52-8.mol
• Article Data: 11

Chemical Properties

• Melting Point: 64-66 °C
• Boiling Point: 401.6±35.0 °C(Predicted)
• Appearance: /
• Density: 1.136±0.06 g/cm3(Predicted)
• PKA: 4.02±0.10(Predicted)
• CAS DataBase Reference: 3,5-BIS(ALLYLOXY)BENZENECARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-BIS(ALLYLOXY)BENZENECARBOXYLIC ACID(185254-52-8)
• EPA Substance Registry System: 3,5-BIS(ALLYLOXY)BENZENECARBOXYLIC ACID(185254-52-8)

Safety Data

• Hazardous Substances Data: 185254-52-8(Hazardous Substances Data)

Upstream product

• 135710-38-2 3,5-bis(2-propen-1-yloxy)benzoic acid methyl ester 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 106-95-6 allyl bromide 
• 189684-08-0 allyl 3,5-bis(allyloxy)benzoate 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 

Downstream Products

• 932380-52-4 3,5-bis(allyloxy)-N-(benzyloxy)benzamide 
• 73338-85-9 5,6-dimethoxy-2-(3-hydroxy-5-methoxyphenyl)benzofuran 
• 1404616-62-1 N-(3,5-(diallyloxy)benzoyl)-8-aminoquinoline 
• 159507-53-6 1,4-bis[3,5-dihydroxybenzoyloxy]benzene 
• 873332-52-6 5'-(3,5-bis(allyloxy)benzoyl)-2',3'-isopropylidene guanosine 
• 1000773-37-4 3,5-bis(allyloxy)benzoic acid chloride 
• 185254-55-1 1,4-bis[3,5-bis(allyloxy)benzoyloxy]benzene 

Relevant articles and documents

Mixing End Groups in Thiol-Ene/Yne Reactions as a Simple Approach toward Multienzyme-Responsive Polymeric Amphiphiles

Taking advantage of the high fidelity of thiol-ene and thiol-yne chemistries, we used mixtures of thiols to prepare degradable PEG-dendron amphiphiles functionalized with two different types of enzymatically cleavable end groups. By tuning the feed ratios of the two thiols, we achieved mixtures of hybrids with statistically different ratios of end groups. Studies of the disassembly of statistically mixed hybrids showed that these amphiphiles have higher degrees of response when incubated with each of the activating enzymes, whereas a greater degree of selectivity was observed for a control mixture of two distinct amphiphiles, which required the presence of both types of enzyme to undergo complete disassembly. The potential to introduce different end groups by using a mixture of thiols in an efficient single thiol-ene or thiol-yne step opens the way for simple modification of various ene- or yne-containing polymers and tailoring of their structural and functional properties.

Synthetic method for moracin F using Suzuki coupling reaction

An objective of the present invention is to provide a method for synthesizing a natural compound moracin F having biological activity. Inventors of the present invention can efficiently synthesize moracin F having biological activity by using Suzuki coupl

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