| Identification | More | [Name]
2-AMINO-4-METHYLQUINOLINE HYDROCHLORIDE | [CAS]
39773-47-2 | [Synonyms]
RARECHEM AK HD C006 TIMTEC-BB SBB000836 DL-beta-(4-bromophenyl)alanine DL-BETA-(P-BROMOPHENYL)ALANINE 3-(P-BROMOPHENYL)-DL-BETA-ALANINE
DL-3-Amino-3-(4-bromo)propanoic acid 2-AMINO-4-METHYLQUINOLINE HYDROCHLORIDE 3-AMINO-3-(4-BROMOPHENYL)PROPANOIC ACID Benzenepropanoic acid, b-aMino-4-broMo- BETA-AMINO-4-BROMO-BENZENEPROPANOIC ACID 3-AMINO-3-(4-BROMO-PHENYL)-PROPIONIC ACID Benzenepropanoic acid, .beta.-amino-4-bromo- DL-3-AMINO-3-(4-BROMO-PHENYL)-PROPIONIC ACID 3-AMino-3-(4-broMophenyl)propionic acid, 97+% (RS)-3-Amino-3-(4-bromophenyl)-propionic acid (RS)-beta-Amino-beta-(4-bromophenyl)propionic acid | [Molecular Formula]
C10H11ClN2 | [MDL Number]
MFCD07700220 | [Molecular Weight]
194.66 | [MOL File]
39773-47-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
235-236°C | [Boiling point ]
378.1±32.0 °C(Predicted) | [density ]
1.585 | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
solid | [pka]
3.62±0.10(Predicted) | [Appearance]
White to off-white Solid | [Sensitive ]
Air Sensitive | [CAS DataBase Reference]
39773-47-2(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Synthesis]
To 30 mL of ethanol was added 5.00 g (27.0 mmol) of p-bromobenzaldehyde, 2.80 g (27.0 mmol) of malonic acid, and 3.10 g (40.2 mmol) of ammonium acetate, and the reaction mixture was refluxed and stirred for 10 hr at 75 to 80°C. The reaction was carried out by stirring the mixture for 1 hr at room temperature. After completion of the reaction, the mixture was continued to be stirred at room temperature for 1 h. Subsequent filtration afforded 4.8 g of DL-3-amino-3-(4-bromophenyl)propionic acid (racemic mixture) in 72.2% isolated yield based on p-bromobenzaldehyde, and the product was a white powder.The physical properties of DL-3-amino-3-(4-bromophenyl)propionic acid (racemic mixture) were as follows:1H-NMR ( δ (ppm), D2O): 2.93 (dd, 1H, J = 17.1, 6.8 Hz), 3.04 (dd, 1H, J = 17.1, 7.8 Hz), 4.63 (dd, 1H, J = 7.8, 6.8 Hz), 7.22 (s, 1H), 7.24 (s, 1H), 7.47 (s, 1H), 7.49 (s, 1H); 13C-NMR (δ (ppm), D2O): 40.4, 53.9, 126.0, 131.9, 135.3, 137.1, 175.9. | [References]
[1] Advanced Synthesis and Catalysis, 2010, vol. 352, # 2-3, p. 395 - 406 [2] Advanced Synthesis and Catalysis, 2017, vol. 359, # 9, p. 1570 - 1576 [3] Patent: EP1621529, 2006, A1. Location in patent: Page/Page column 33 [4] European Journal of Medicinal Chemistry, 2018, vol. 156, p. 252 - 268 [5] Journal of the Chemical Society. Perkin Transactions 1, 2001, # 14, p. 1673 - 1695 |
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