75865-45-1

Basic information

• Product Name: 4-BROMO-2,3,5,6-TETRAFLUOROBENZYLALCOHOL
• Synonyms: 4-BROMO-2,3,5,6-TETRAFLUOROBENZYLALCOHOL;(4-bromo-2,3,5,6-tetrafluorophenyl)methanol
• CAS NO: 75865-45-1
• Molecular Formula: C₇H₃BrF₄O
• Molecular Weight: 258.9957328
• Mol File: 75865-45-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 231.4 °C at 760 mmHg
• Flash Point: 93.7 °C
• Appearance: /
• Density: 1.9 g/cm³
• Vapor Pressure: 0.0349mmHg at 25°C
• Refractive Index: 1.504
• CAS DataBase Reference: 4-BROMO-2,3,5,6-TETRAFLUOROBENZYLALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-2,3,5,6-TETRAFLUOROBENZYLALCOHOL(75865-45-1)
• EPA Substance Registry System: 4-BROMO-2,3,5,6-TETRAFLUOROBENZYLALCOHOL(75865-45-1)

Safety Data

• Hazardous Substances Data: 75865-45-1(Hazardous Substances Data)

Usage

General Description

4-Bromo-2,3,5,6-tetrafluorobenzylalcohol is a compound with the chemical formula C7H4BrF4O. It is a derivative of benzylalcohol, with bromine and fluoride atoms attached to the benzene ring. 4-BROMO-2,3,5,6-TETRAFLUOROBENZYLALCOHOL is commonly used as a building block in organic synthesis and pharmaceutical research. It has been found to possess antimicrobial and antifungal properties, making it a potential candidate for the development of new pharmaceutical drugs. Additionally, it is also used in the production of various chemicals and materials in the industry. Overall, 4-Bromo-2,3,5,6-tetrafluorobenzylalcohol is a versatile compound with a range of useful applications in different fields.

InChI:InChI=1/C7H3BrF4O/c8-3-6(11)4(9)2(1-13)5(10)7(3)12/h13H,1H2

Upstream product

• 108574-98-7 formyl-2,3,5,6-tetrafluoro-1-bromobenzene 
• 653-37-2 perfluorobenzaldehyde 

Downstream Products

• 1013095-20-9 (4-bromo-2,3,5,6-tetrafluorobenzyloxy)-tert-butyldimethylsilane 

Relevant articles and documents

Functionalised phosphonate ester supported lanthanide (Ln = La, Nd, Dy, Er) complexes

A series of phosphonate ester supported lanthanide complexes bearing functionalities for subsequent immobilisation on semiconductor surfaces are prepared. Six phosphonate ester ligands (L1-L6) with varying aromatic residues are synthesised. Subsequent com

Method for producing cyclopropanecarboxylates

There is provided a method for producing a cyclopropanecarboxylate of formula (1): 1which comprises contacting a cyclopropanecarboxylate of formula (2): 2with a monohydroxy compound of formula (3):R7OH??(3)in the presence of a lithium compound of formula (4):R8OLi??(4),wherein R1, R2, R3, R4 and R5 each independently represent a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, or a substituted or unsubstituted aryl group; R6 represents an alkyl group having 1 to 10 carbon atoms or a substituted or unsubstituted phenyl group; R7 and R8 do not simultaneously represent the same and each independently represent a substituted or unsubstituted alkyl group, or a substituted or unsubstituted aryl group.