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ChemicalBook > CAS DataBase List > 3-FLUORO-4-METHYLANISOLE

3-FLUORO-4-METHYLANISOLE

Application
Product Name
3-FLUORO-4-METHYLANISOLE
CAS No.
405-06-1
Chemical Name
3-FLUORO-4-METHYLANISOLE
Synonyms
3-FLUORO-4-METHYLANISOLE;2-Fluoro-4-methoxytoluene;3-Fluoro-4-methylanisole99%;3-Fluoro-4-methylanisole 99%;3-Fluoro-4-Methylbenzyl Ether;2-Fluoro-4-Methoxy-1-Methylbenzene;Benzene, 2-fluoro-4-methoxy-1-methyl-;3-FLUORO-4-METHYLANISOLE ISO 9001:2015 REACH;3-Fluoro-4-Methylanisole[2-Fluoro-4-Methoxytoluene];1-Fluoro-3-methoxy-6-methylbenzene-Fluoro-4-methoxytoluene
CBNumber
CB1470721
Molecular Formula
C8H9FO
Formula Weight
140.15
MOL File
405-06-1.mol
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3-FLUORO-4-METHYLANISOLE Property

Boiling point:
63.5-64°C
Density 
1.046±0.06 g/cm3(Predicted)
refractive index 
1.4909
storage temp. 
Sealed in dry,Room Temperature
Appearance
Colorless to light yellow Liquid
CAS DataBase Reference
405-06-1(CAS DataBase Reference)
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Safety

Hazard Codes 
F
Risk Statements 
36/37/38
Safety Statements 
26-36
Hazard Note 
Flammable
HS Code 
2909309090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

TRC
Product number
F597018
Product name
3-Fluoro-4-methylanisole
Packaging
1g
Price
$75
Updated
2021/12/16
Apolloscientific
Product number
PC8219
Product name
3-Fluoro-4-methylanisole
Purity
99%
Packaging
1g
Price
$16
Updated
2021/12/16
SynQuest Laboratories
Product number
2707-3-X5
Product name
3-Fluoro-4-methylanisole
Purity
99%
Packaging
1g
Price
$25
Updated
2021/12/16
AK Scientific
Product number
X4255
Product name
3-Fluoro-4-methylanisole
Packaging
1g
Price
$31
Updated
2021/12/16
Apolloscientific
Product number
PC8219
Product name
3-Fluoro-4-methylanisole
Purity
99%
Packaging
5g
Price
$52
Updated
2021/12/16
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3-FLUORO-4-METHYLANISOLE Chemical Properties,Usage,Production

Application

Studies have reported that 3-fluoro-4-methyl anisole can be used to prepare a diarylphosphine ligand, L10b.

Reactions

3-Fluoro-4-methylanisole is a nucleophilic, ring substituted electron acceptor that can be activated by electron donors. The nitro group and the electron donating substituents on the ring are important for this reactivity. 3-Fluoro-4-methylanisole can form substitution products with methyl or formyl groups in the presence of a strong base such as palladium, 3-fluoro-4-methylphenol, or nitro groups. This reactivity is regiospecific, meaning that the substitution will only occur at one of two possible sites on the ring. 3-Fluoro-4-methylanisole's chemical properties give it both activating and deactivating properties in organic reactions.

Synthesis

50868-72-9

405-06-1

The general procedure for the synthesis of 3-fluoro-4-methylanisole from 5-methoxy-2-methylaniline was as follows: a mixed system of 5-methoxy-2-methylaniline (5.0 g; 36 mmol), concentrated hydrochloric acid (7.6 mL, 12 M solution; 91 mmol), and deionized water (11 mL) was heated and stirred at 60 °C for 15 min until complete dissolution. After the reaction solution was cooled to 0 °C, aqueous sodium nitrite (2.5 g; 36 mmol) was slowly added dropwise to control the internal temperature ≤7 °C. The reaction solution was then stirred at 0 °C for 15 min. The reaction solution was continued to be stirred at 0 °C for 30 min, followed by cautious addition of pre-cooled tetrafluoroboric acid solution (5.3 mL, 48% solution; 40 mmol). The reaction mixture was stirred at 0 °C for 20 min before the resulting brown solid was collected by filtration and washed sequentially with ice water (3 × 10 mL) and deionized water (2 × 10 mL). The solid was dried under high vacuum for 20 h. The solid was then heated with a heat gun until the release of white fumes of boron trifluoride was stopped. The resulting brown oil was extracted with ethyl acetate and water in liquid-liquid extraction, and the organic phase was dried with anhydrous sodium sulfate and concentrated under reduced pressure, and finally purified by short distillation to obtain the colorless oily product 3-fluoro-4-methylanisole (1.6 g; 31% yield).

References

[1] Patent: US6414002, 2002, B1

3-FLUORO-4-METHYLANISOLE Preparation Products And Raw materials

Raw materials

Preparation Products

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3-FLUORO-4-METHYLANISOLE Suppliers

ecochem international chemical broker
Tel
--
Fax
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Email
export@ecochem.dk
Country
Europe
ProdList
6371
Advantage
66
kemikalieimport
Tel
--
Fax
--
Email
Sales@kemikalieimport.dk
Country
Europe
ProdList
6685
Advantage
47
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View Lastest Price from 3-FLUORO-4-METHYLANISOLE manufacturers

Hebei Chuanghai Biotechnology Co., Ltd
Product
3-FLUORO-4-METHYLANISOLE 405-06-1
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-26
Honest Joy Holdings Limited
Product
3-Fluoro-4-methylanisole 405-06-1
Price
US $0.00/KG
Min. Order
1KG
Purity
99.3%
Supply Ability
100 tons
Release date
2022-02-21
Career Henan Chemical Co
Product
2-Fluoro-4-methoxy-1-methylbenzene 405-06-1
Price
US $1.00/g
Min. Order
1g
Purity
99%
Supply Ability
10000KGS
Release date
2020-01-09

405-06-1, 3-FLUORO-4-METHYLANISOLERelated Search:


  • 3-FLUORO-4-METHYLANISOLE
  • 2-Fluoro-4-methoxytoluene
  • 3-Fluoro-4-methylanisole 99%
  • 3-Fluoro-4-methylanisole99%
  • 2-Fluoro-4-Methoxy-1-Methylbenzene
  • 2-Fluoro-4-methoxytoluene, 2-Fluoro-4-methoxy-1-methylbenzene, 3-Fluoro-4-methylphenyl methyl ether
  • 3-Fluoro-4-Methylanisole[2-Fluoro-4-Methoxytoluene]
  • 1-Fluoro-3-methoxy-6-methylbenzene,2-Fluoro-4-methoxytoluene
  • 1-Fluoro-3-methoxy-6-methylbenzene-Fluoro-4-methoxytoluene
  • Benzene, 2-fluoro-4-methoxy-1-methyl-
  • 3-FLUORO-4-METHYLANISOLE ISO 9001:2015 REACH
  • 3-Fluoro-4-Methylbenzyl Ether
  • 405-06-1
  • Aromatic Halides (substituted)
  • Anisole
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Fluorine Compounds