4-(1-AMINO-ETHYL)-BENZOIC ACID METHYL ESTER
- Product Name
- 4-(1-AMINO-ETHYL)-BENZOIC ACID METHYL ESTER
- CAS No.
- 80051-07-6
- Chemical Name
- 4-(1-AMINO-ETHYL)-BENZOIC ACID METHYL ESTER
- Synonyms
- Methyl 4-(1-aMinoethyl)benzoate;4-(1-AMINO-ETHYL)-BENZOIC ACID METHYL ESTER;Benzoic acid, 4-(1-aminoethyl)-, methyl ester
- CBNumber
- CB52459685
- Molecular Formula
- C10H13NO2
- Formula Weight
- 179.22
- MOL File
- 80051-07-6.mol
4-(1-AMINO-ETHYL)-BENZOIC ACID METHYL ESTER Property
- Boiling point:
- 281.5±15.0 °C(Predicted)
- Density
- 1.089±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 8?+-.0.10(Predicted)
- Appearance
- Colorless to off-white Solid-liquid mixture
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
- M328533
- Product name
- Methyl4-(1-aminoethyl)benzoate
- Packaging
- 250mg
- Price
- $165
- Updated
- 2021/12/16
- Product number
- CS-M0171
- Product name
- methyl4-(1-aminoethyl)benzoate
- Purity
- ≥97.0%
- Packaging
- 250mg
- Price
- $75
- Updated
- 2021/12/16
- Product number
- CS-M0171
- Product name
- methyl4-(1-aminoethyl)benzoate
- Purity
- ≥97.0%
- Packaging
- 100mg
- Price
- $102
- Updated
- 2021/12/16
- Product number
- 3829AH
- Product name
- Methyl4-(1-aminoethyl)benzoate
- Packaging
- 250mg
- Price
- $162
- Updated
- 2021/12/16
- Product number
- CS-M0171
- Product name
- methyl4-(1-aminoethyl)benzoate
- Purity
- ≥97.0%
- Packaging
- 1g
- Price
- $188
- Updated
- 2021/12/16
4-(1-AMINO-ETHYL)-BENZOIC ACID METHYL ESTER Chemical Properties,Usage,Production
Synthesis
3609-53-8
593-51-1
74-89-5
80051-07-6
GENERAL STEPS: Methyl 4-acetylbenzoate (1.07 g, 6 mmol), methylamine (33% ethanol solution, 4.5 mL), methylamine hydrochloride (1.62 g, 24.0 mmol), and sodium cyanoborohydride (0.56 g, 9.0 mmol) were dissolved in a solvent mixture of tetrahydrofuran (12 mL) and methanol (7 mL). The reaction mixture was stirred at 65 °C for 16 hours. Upon completion of the reaction, the reaction solution was concentrated in vacuum and the residue was redissolved in dichloromethane (20 mL) and washed with deionized water (20 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated in vacuum to give the crude methyl 4-(1-aminoethyl)benzoate, which could be used in the next reaction without further purification. Yield: 0.86 g, 75% yield. LCMS analysis (Method B): retention time 0.98 min, purity 89%; m/z 194.05 ([M+H]+, 100%).
References
[1] Patent: WO2010/20556, 2010, A1. Location in patent: Page/Page column 169-170
4-(1-AMINO-ETHYL)-BENZOIC ACID METHYL ESTER Preparation Products And Raw materials
Raw materials
Preparation Products
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