4-fluorobicyclo[2.2.2]octane-1-carboxylic acid
- Product Name
- 4-fluorobicyclo[2.2.2]octane-1-carboxylic acid
- CAS No.
- 78385-84-9
- Chemical Name
- 4-fluorobicyclo[2.2.2]octane-1-carboxylic acid
- Synonyms
- 4-fluorobicyclo[2.2.2]octane-1-carboxylic acid;Bicyclo[2.2.2]octane-1-carboxylic acid, 4-fluoro-
- CBNumber
- CB32668812
- Molecular Formula
- C9H13FO2
- Formula Weight
- 172.2
- MOL File
- 78385-84-9.mol
4-fluorobicyclo[2.2.2]octane-1-carboxylic acid Property
- storage temp.
- 2-8°C
- Appearance
- White Powder
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
- AS56728
- Product name
- 4-Fluorobicyclo[2.2.2]octane-1-carboxylic acid
- Purity
- 97+%
- Packaging
- 100mg
- Price
- $414
- Updated
- 2021/12/16
- Product number
- HCH0418992
- Product name
- 4-FLUOROBICYCLO[2.2.2]OCTANE-1-CARBOXYLIC ACID
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $451.86
- Updated
- 2021/12/16
- Product number
- 0901CU
- Product name
- 4-Fluorobicyclo[2.2.2]octane-1-carboxylicacid
- Packaging
- 250mg
- Price
- $901
- Updated
- 2021/12/16
- Product number
- 0901CU
- Product name
- 4-Fluorobicyclo[2.2.2]octane-1-carboxylicacid
- Packaging
- 500mg
- Price
- $1363
- Updated
- 2021/12/16
- Product number
- 122478
- Product name
- 4-Fluorobicyclo[2.2.2]octane-1-carboxylicacid
- Purity
- 97.0%
- Packaging
- 1g
- Price
- $4752
- Updated
- 2021/12/16
4-fluorobicyclo[2.2.2]octane-1-carboxylic acid Chemical Properties,Usage,Production
Synthesis
78385-85-0
78385-84-9
The general procedure for the synthesis of 4-fluorodicyclo[2.2.2]octane-1-carboxylic acid from the compound (CAS: 78385-85-0) is as follows: Preparation of intermediate A51C: To a solution of intermediate A51B (80 mg, 0.430 mmol) in methanol (2 mL) was added slowly and dropwise 1 M sodium hydroxide solution (1 mL, 1.00 mmol). The reaction mixture was stirred overnight at room temperature and subsequently concentrated. The residue was acidified with 1 N hydrochloric acid to pH about 2 and subsequently extracted with ethyl acetate. The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and filtered. Concentration of the filtrate gave the intermediate A51C (66 mg, 89% yield) as a white solid, which could be used in the next step of the reaction without further purification. 1H NMR (400 MHz, methanol-d4) δ ppm: 2.10-1.95 (m, 6H), 1.90-1.78 (m, 6H).
References
[1] Journal of Organic Chemistry, 1982, vol. 47, # 15, p. 2951 - 2957
[2] Patent: US9273058, 2016, B2. Location in patent: Page/Page column 529
4-fluorobicyclo[2.2.2]octane-1-carboxylic acid Preparation Products And Raw materials
Raw materials
Preparation Products
4-fluorobicyclo[2.2.2]octane-1-carboxylic acid Suppliers
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