37116-80-6

Basic information

• Product Name: lunularin
• Synonyms: lunularin;1-(3-Hydroxyphenyl)-2-(4-hydroxyphenyl)ethane;3,4'-Ethylenebisphenol;4-[2-(3-Hydroxyphenyl)ethyl]phenol;3-[2-(4-hydroxyphenyl)ethyl]phenol;3-(4-hydroxyphenethyl)phenol
• CAS NO: 37116-80-6
• Molecular Formula: C₁₄H₁₄O₂
• Molecular Weight: 214.2598
• Mol File: 37116-80-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 382°Cat760mmHg
• Flash Point: 185°C
• Appearance: /
• Density: 1.191g/cm³
• Vapor Pressure: 2.22E-06mmHg at 25°C
• Refractive Index: 1.63
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: lunularin(CAS DataBase Reference)
• NIST Chemistry Reference: lunularin(37116-80-6)
• EPA Substance Registry System: lunularin(37116-80-6)

Safety Data

• Hazardous Substances Data: 37116-80-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H14O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-3,6-10,15-16H,4-5H2

Upstream product

• 23255-59-6 lunularic acid 
• 52528-97-9 1-methoxy-3-(4-methoxyphenethyl)benzene 
• 491-79-2 Hydrangeaic acid 
• 6971-51-3 3-methoxybenzyl alcohol 
• 88075-18-7 4-(2-(trimethylsilyl)ethynyl)phenol 
• 2200-91-1 4-ethynylphenol 
• 626-02-8 3-Iodophenol 
• 540-38-5 p-Iodophenol 
• 39032-14-9 3,4'-Dimethoxystilben 
• 60815-18-1 diethyl [(3-methoxyphenyl)methyl]phosphonate 
• 874-98-6 1-bromomethyl-3-methoxybenzene 
• 591-31-1 3-methoxy-benzaldehyde 
• 39032-14-9 1-[(E)-2-(4-methoxyphenyl)ethenyl]-3-methoxybenzene 
• 104-47-2 p-methoxybenzylnitrile 

Downstream Products

• 89911-97-7 perrottetine E 
• 52528-89-9 3,4'-bis-benzoyloxy-bibenzyl 
• 111439-38-4 1,2,8-trihydroxy-9-oxo-4-phenethyl-9H-benzocycloheptene-6-carboxylic acid 

Relevant articles and documents

Chromium-Salen Complex/Nitroxyl Radical Cooperative Catalysis: A Combination for Aerobic Intramolecular Dearomative Coupling of Phenols

We describe an aerobic intramolecular dearomative coupling reaction of tethered phenols using a catalytic system consisting of a chromium-salen (Cr-salen) complex combined with a nitroxyl radical. This novel catalytic system enables formation of various spirocyclic dienone products including those unable to be accessed by previously reported methods efficiently under mild reaction conditions.

Riccardin C derivatives as anti-MRSA agents: Structure-activity relationship of a series of hydroxylated bis(bibenzyl)s

Members of a series of macrocyclic bis(bibenzyl) riccardin-class derivatives were found to exhibit antibacterial activity towards methicillin-resistant Staphylococcus aureus (anti-MRSA activity). Structure-activity relationship (SAR) studies were conducted, focusing on the number and position of the hydroxyl groups. The minimum essential structure for anti-MRSA activity was also investigated.