(2S)-2-AMINO-2-(3-FLUOROPHENYL)ETHAN-1-OL HCL
- Product Name
- (2S)-2-AMINO-2-(3-FLUOROPHENYL)ETHAN-1-OL HCL
- CAS No.
- 1240480-36-7
- Chemical Name
- (2S)-2-AMINO-2-(3-FLUOROPHENYL)ETHAN-1-OL HCL
- Synonyms
- (S)-2-AMINO-2-(3-FLUOROPHENYL)ETHANOL HCL;(2S)-2-AMINO-2-(3-FLUOROPHENYL)ETHAN-1-OL HCL;(S)-2-Amino-2-(3-fluorophenyl)ethanol hydrochloride;(S)-2-Amino-2-(3-fluorophenyl)ethan-1-ol hydrochloride;(2S)-2-AMINO-2-(3-FLUOROPHENYL)ETHAN-1-OL HYDROCHLRIDE
- CBNumber
- CB53153535
- Molecular Formula
- C8H11ClFNO
- Formula Weight
- 191.6304432
- MOL File
- 1240480-36-7.mol
(2S)-2-AMINO-2-(3-FLUOROPHENYL)ETHAN-1-OL HCL Property
- storage temp.
- Inert atmosphere,Room Temperature
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
- 6154DT
- Product name
- (S)-2-Amino-2-(3-fluorophenyl)ethanolhydrochloride
- Packaging
- 5g
- Price
- $2085
- Updated
- 2021/12/16
- Product number
- A143270
- Product name
- (S)-2-Amino-2-(3-fluorophenyl)ethanolhydrochloride
- Purity
- 97%
- Packaging
- 100mg
- Price
- $58
- Updated
- 2021/12/16
- Product number
- A143270
- Product name
- (S)-2-Amino-2-(3-fluorophenyl)ethanolhydrochloride
- Purity
- 97%
- Packaging
- 250mg
- Price
- $87
- Updated
- 2021/12/16
- Product number
- A143270
- Product name
- (S)-2-Amino-2-(3-fluorophenyl)ethanolhydrochloride
- Purity
- 97%
- Packaging
- 1g
- Price
- $214
- Updated
- 2021/12/16
- Product number
- CM248432
- Product name
- (S)-2-Amino-2-(3-fluorophenyl)ethanolhydrochloride
- Purity
- 95+%
- Packaging
- 1g
- Price
- $486
- Updated
- 2021/12/16
(2S)-2-AMINO-2-(3-FLUOROPHENYL)ETHAN-1-OL HCL Chemical Properties,Usage,Production
Synthesis
1312719-10-0
1240480-36-7
GENERAL METHODOLOGY: Step 4: To a solution of compound 60 (3.0 g, 8.0 mmol) in methanol (100 mL) was added a methanol solution of 3N hydrochloric acid (8.0 mL, 24 mmol). The reaction mixture was stirred at room temperature for 1 hour and then concentrated under reduced pressure by rotary evaporator. The concentrate was diluted with ethyl acetate (30 mL) and subsequently filtered to collect the solid. The solid was washed with ethyl acetate (20 mL) to afford compound 62a (880 mg, 57% yield) as a white solid. The product was characterized by 1H NMR (500 MHz, CD3OD): δ 7.50 (m, 1H), 7.32-7.28 (m, 2H), 7.19 (m, 1H), 7.41 (m, 1H), 3.93 (m, 1H), 3.82 (m, 1H). lcms (ESI) m/z: 156.1 [M+H]+.
References
[1] Patent: US2014/66453, 2014, A1. Location in patent: Paragraph 0218-0219
(2S)-2-AMINO-2-(3-FLUOROPHENYL)ETHAN-1-OL HCL Preparation Products And Raw materials
Raw materials
Preparation Products
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