methyl 2-fluoro-4-methylbenzoate
- Product Name
- methyl 2-fluoro-4-methylbenzoate
- CAS No.
- 74733-29-2
- Chemical Name
- methyl 2-fluoro-4-methylbenzoate
- Synonyms
- methyl 2-fluoro-4-methylbenzoate;2-Fluoro-4-Methyl-benzoic acid Methyl ester;methyl 2-fluoro-4-methylbenzoate - [AC78605];Benzoic acid, 2-fluoro-4-methyl-, methyl ester
- CBNumber
- CB91561260
- Molecular Formula
- C9H9FO2
- Formula Weight
- 168.16
- MOL File
- 74733-29-2.mol
methyl 2-fluoro-4-methylbenzoate Property
- Boiling point:
- 226.8±28.0 °C(Predicted)
- Density
- 1.137±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- White to off-white Solid
Safety
- HS Code
- 2916399090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- M321645
- Product name
- Methyl2-Fluoro-4-methylbenzoate
- Packaging
- 250mg
- Price
- $75
- Updated
- 2021/12/16
- Product number
- HCH0044528
- Product name
- METHYL 2-FLUORO-4-METHYLBENZOATE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $503.64
- Updated
- 2021/12/16
- Product number
- PC909749
- Product name
- Methyl2-fluoro-4-methylbenzoate
- Purity
- 95%
- Packaging
- 25g
- Price
- $833
- Updated
- 2021/12/16
- Product number
- 74733292
- Product name
- Methyl2-fluoro-4-methylbenzoate
- Packaging
- 500mg
- Price
- $863.9
- Updated
- 2021/12/16
- Product number
- 74733292
- Product name
- Methyl2-fluoro-4-methylbenzoate
- Packaging
- 1g
- Price
- $1445.3
- Updated
- 2021/12/16
methyl 2-fluoro-4-methylbenzoate Chemical Properties,Usage,Production
Synthesis
67-56-1
7697-23-6
74733-29-2
(f) Methyl 2-fluoro-4-methylbenzoate (5): Method A: To a mixture of 2-fluoro-4-methylbenzoic acid (2.0 g, 13.0 mmol) and K2CO3 (3.6 g, 26.0 mmol) in acetonitrile (15 mL) was added CH3I (1.6 mL, 25.6 mmol) dropwise with stirring. The reaction mixture was heated to reflux overnight and the solvent was removed by distillation under reduced pressure. The residue was dissolved with EtOAc, washed sequentially with water and saturated saline, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography with hexane/EtOAc (6:1) as eluent to give a white solid 5 (1.73 g, 79% yield) with melting point 51-53 °C.1H NMR (CDCl3) δ: 7.83 (t, J=8.0 Hz, 1H), 7.00 (dd, J=8.0,1.0 Hz, 1H), 6.95 (d, J= 12.0 Hz, 1H), 3.91 (s, 3H), 2.39 (s, 3H). Method B: Concentrated sulfuric acid (5 mL) was added dropwise to a solution of 2-fluoro-4-methylbenzoic acid (7.0 g, 45.4 mmol) in MeOH (100 mL) under stirring. The reaction mixture was heated to reflux overnight and then the solvent was removed by distillation under reduced pressure. The residue was dissolved with EtOAc, washed with saturated aqueous NaHCO3 and saturated saline in turn, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography with hexane/EtOAc (6:1) as eluent to give white solid 5 (6.88 g, 90% yield). The analytical data were the same as that of Method A.
References
[1] Patent: WO2010/116270, 2010, A1. Location in patent: Page/Page column 55
[2] Organic Process Research and Development, 2011, vol. 15, # 3, p. 565 - 569
[3] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 7, p. 1742 - 1747
[4] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 24, # 7, p. 1742 - 1747
[5] Patent: EP1449844, 2004, A1. Location in patent: Page 22
methyl 2-fluoro-4-methylbenzoate Preparation Products And Raw materials
Raw materials
Preparation Products
methyl 2-fluoro-4-methylbenzoate Suppliers
- Tel
- 0519-89803565 13776850645
- Fax
- 0519-89803575
- info4@huanlingchem.com
- Country
- China
- ProdList
- 983
- Advantage
- 68
- Tel
- 400-6009262 15618770481
- Fax
- 021-64823266
- yhx@titansci.com
- Country
- China
- ProdList
- 14101
- Advantage
- 59
- Tel
- 021-58170097
- info@topbiochem.com
- Country
- China
- ProdList
- 9520
- Advantage
- 58
- Tel
- 86(512)5235 8471 17715136450
- Fax
- 86(512)5235 6881
- sales@shiyabiopharm.com
- Country
- China
- ProdList
- 4169
- Advantage
- 58
- Tel
- 029-86115547 17791676824
- Fax
- 02151602123
- sales@cochemical.com
- Country
- China
- ProdList
- 3014
- Advantage
- 58
- Tel
- 021-11111111 11111111111
- Fax
- qq:546919421
- 546919421@qq.com
- Country
- China
- ProdList
- 3660
- Advantage
- 55
- Tel
- sales@ahpharmatech.com
- Country
- China
- ProdList
- 5734
- Advantage
- 55
- Tel
- 0512-63009836 18994340901
- Fax
- 0512-63006936
- helen@struchem.com
- Country
- China
- ProdList
- 3979
- Advantage
- 60
- Tel
- 025-83453382-8005
- Fax
- 025-83453382
- sale@parabiochem.com
- Country
- China
- ProdList
- 9595
- Advantage
- 55
- Tel
- 571-89925085
- Fax
- 0086-571-89925065
- sales@amadischem.com
- Country
- China
- ProdList
- 131957
- Advantage
- 58