ChemicalBook > Product Catalog >Organic Chemistry >Alcohols,Phenols,Phenol alcohols >3-Fluoro-4-methylphenol

3-Fluoro-4-methylphenol

3-Fluoro-4-methylphenol Suppliers list
Company Name: Shandong Youfu Pharmaceutical Technology Co., Ltd.  Gold
Tel: +86-0536-8226195 +86-13953676784
Email: lee@unipharm-sd.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: TCI (Shanghai) Development Co., Ltd.  
Tel: 021-67121386
Email: Sales-CN@TCIchemicals.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com

3-Fluoro-4-methylphenol manufacturers

3-Fluoro-4-methylphenol Basic information
Product Name:3-Fluoro-4-methylphenol
Synonyms:2-Fluoro-4-hydroxytoluene;3-FLUORO-4-METHYLPHENOL;3-FLUORO-P-CRESOL;3-Fluoro-p-cresol (OH=1);3-Fluoro-4-methylphenol, JRD,;3-Fluoro-p-cresol>;Phenol, 3-fluoro-4-methyl-
CAS:452-78-8
MF:C7H7FO
MW:126.13
EINECS:200-110-4
Product Categories:Fluorine series;Aromatic Phenols;Phenol&Thiophenol&Mercaptan;Fluorine Compounds;Phenols
Mol File:452-78-8.mol
3-Fluoro-4-methylphenol Structure
3-Fluoro-4-methylphenol Chemical Properties
Melting point 72 °C
Boiling point 196 °C
density 1.17
refractive index 1.5150
Fp 29 °C
storage temp. Inert atmosphere,Room Temperature
pka9.27±0.18(Predicted)
form powder to lump
color White to Light yellow to Light orange
OdorPhenol-like
InChIInChI=1S/C7H7FO/c1-5-2-3-6(9)4-7(5)8/h2-4,9H,1H3
InChIKeyGJOOCAXPERKNMN-UHFFFAOYSA-N
SMILESC1(O)=CC=C(C)C(F)=C1
CAS DataBase Reference452-78-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 21/22-34-52-36-22
Safety Statements 26-36/37/39-60-45
RIDADR 2922
WGK Germany WGK 3
Hazard Note Irritant
HazardClass 8
HS Code 29081990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Chronic 3
Eye Irrit. 2
MSDS Information
3-Fluoro-4-methylphenol Usage And Synthesis
Uses3-Fluoro-4-methylphenol is a phenolic derivative and can be used as a pharmaceutical intermediate.
Synthesis3-Fluoro-4-methylaniline (5g, 39.95Immol) was dissolved in 10% sulfuric acid aqueous solution (100ml). Thereafter, the temperature was lowered to 0°C. thereto sodium nitrate (5.5g, 79.902mmol) was added, and the reaction mixture was stirred at same temperature for 30 minutes. Then the reaction mixture was stirred at 50°C for 30 minutes, and the last time, stirred at 80°C for 5 hours. Ice water was added to quench the reaction, and aqueous layer was extracted with ethyl acetate. Combined organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography (n-hexane:ethyl acetate = 8:1) to give 2.26g (yield: 44.8%, colorless oil) of the target compound. 3-fluoro-4-methylphenol, yield 2.26g, 44.8% 1H NMR(400MHz, CDCl3): 6.98(1, J=8.6Hz, 1H), 6.52(m, 2H), 5.82(br, 1H), 2.12(s, 3H).
3-Fluoro-4-methylphenol synthesis
References[1] Patent: WO2007/8037, 2007, A1. Location in patent: Page/Page column 34-35
[2] Journal of the Chemical Society, 1949, p. Spl. 113
[3] Journal of the American Chemical Society, 1950, vol. 72, p. 1806
3-Fluoro-4-methylphenol Preparation Products And Raw materials
Raw materials3-Fluoro-4-methylaniline-->3-Fluoro-4-methylanisole
Preparation Products3-Fluoro-4-methylanisole-->2-Fluoro-4-methoxybenzoic acid-->4-Ethoxy-2-fluorotoluene
Tag:3-Fluoro-4-methylphenol(452-78-8) Related Product Information
3-Fluoro-5-methylbenzonitrile 2,3,5,6-Tetrafluoro-4-hydroxy-benzoic acid 2'-Fluoro-4'-hydroxyacetophenone 5-FLUORO-2-METHYLPHENOL,5-Fluoro-2-methylphenol,98%,5-Fluoro-2-methylphenol 98% 2-Fluoro-4-methoxyacetophenone 3-Fluoro-2-methylphenol 4-Fluoro-3-methylphenol 4-Fluoro-2-methylphenol 6-Fluoroveratraldehyde Octafluoro-4,4'-biphenol 2-Fluoro-4-methylphenol 2-Fluoro-5-methylphenol 2-Chloro-6-fluoro-3-methylphenol 6-Chloro-2-fluoro-3-methylphenol 2-Fluoro-L-tyrosine 4,4'-Dimethoxyoctafluorobiphenyl 2,3,5,6-Tetrafluoro-4-(pentafluorophenyl)phenol 2'-Fluoro-4'-propoxyacetophenone