424803-19-0

Basic information

• Product Name: [5-[3,5-DI(TRIFLUOROMETHYL)PHENYL]-2-FURYL]METHANOL
• Synonyms: ASISCHEM A78094;[5-[3,5-DI(TRIFLUOROMETHYL)PHENYL]-2-FURYL]METHANOL;AKOS BB-7742;RARECHEM AL BD 1035;VITAS-BB TBB000573;ZERENEX E/5017744;{5-[3,5-bis(trifluoromethyl)phenyl]furan-2-yl}methanol
• CAS NO: 424803-19-0
• Molecular Formula: C₁₃H₈F₆O₂
• Molecular Weight: 310.19
• Mol File: 424803-19-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 110 °C
• Boiling Point: 296.4°C at 760 mmHg
• Flash Point: 133.1°C
• Appearance: /
• Density: 1.42g/cm³
• Vapor Pressure: 0.000648mmHg at 25°C
• Refractive Index: 1.457
• CAS DataBase Reference: [5-[3,5-DI(TRIFLUOROMETHYL)PHENYL]-2-FURYL]METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: [5-[3,5-DI(TRIFLUOROMETHYL)PHENYL]-2-FURYL]METHANOL(424803-19-0)
• EPA Substance Registry System: [5-[3,5-DI(TRIFLUOROMETHYL)PHENYL]-2-FURYL]METHANOL(424803-19-0)

Safety Data

• Hazardous Substances Data: 424803-19-0(Hazardous Substances Data)

Usage

General Description

The chemical compound "[5-[3,5-DI(TRIFLUOROMETHYL)PHENYL]-2-FURYL]METHANOL" is a complex molecule that consists of a furan ring with a phenol group attached to it, as well as a trifluoromethyl-substituted phenyl ring. [5-[3,5-DI(TRIFLUOROMETHYL)PHENYL]-2-FURYL]METHANOL is used in various research and industrial applications, such as in the synthesis of pharmaceuticals, agrochemicals, and materials science. The trifluoromethyl group on the phenyl ring makes the compound highly stable and resistant to chemical degradation, while the furan ring provides reactivity and potential for functionalization. Overall, the compound has potential for diverse applications in the fields of chemistry and biology.

InChI:InChI=1/C13H8F6O2/c14-12(15,16)8-3-7(4-9(5-8)13(17,18)19)11-2-1-10(6-20)21-11/h1-5,20H,6H2

Upstream product

• 256658-04-5 5-(3,5-bis(trifluoromethyl)phenyl)furan-2-carbaldehyde 
• 1899-24-7 5-bromo-2-furancarboxaldehyde 
• 73852-19-4 3,5-bis-trifluromethylphenylboronic acid 
• 98-00-0 (2-furyl)methyl alcohol 
• 328-70-1 3,6-bis(trifluoromethyl)bromobenzene 
• 127-08-2 potassium acetate 

Downstream Products

• 1198181-59-7 ethyl ({5-[3,5-bis(trifluoromethyl)phenyl]furan-2-yl}methoxy)acetate 
• 1198181-60-0 ethyl ({5-[3,5-bis(trifluoromethyl)phenyl]tetrahydrofuran-2-yl}methoxy)acetate 
• 1198181-61-1 2-[3,5-bis(trifluoromethyl)phenyl]-5-(chloromethyl)furan 
• 1198181-62-2 {5-[3,5-bis(trifluoromethyl)phenyl]furan-2-yl}acetonitrile 
• 1198181-63-3 {5-[3,5-bis(trifluoromethyl)phenyl]furan-2-yl}acetic acid 
• 1198180-65-2 ({5-[3,5-bis(trifluoromethyl)phenyl]tetrahydrofuran-2-yl}methoxy)acetic acid 
• 1198180-66-3 {5-[3,5-bis(trifluoromethyl)phenyl]tetrahydrofuran-2-yl}acetic acid 

Relevant articles and documents

The Influence of Substitution on Thiol-Induced Oxanorbornadiene Fragmentation

Oxanorbornadienes (ONDs) undergo facile Michael addition with thiols and then fragment by a retro-Diels-Alder (rDA) reaction, a unique two-step sequence among electrophilic cleavable linkages. The rDA reaction rate was explored as a function of the furan

HETEROCYCLIC COMPOUND

The present invention relates to a compound represented by wherein each symbol is as defined in the specification, a salt thereof and the like.