ChemicalBook--->CAS DataBase List--->39773-47-2

39773-47-2

39773-47-2 Structure

39773-47-2 Structure
IdentificationMore
[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 PropertiesBack 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)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[Risk Statements ]

41
[Safety Statements ]

26-39
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2921490090
Spectrum DetailBack Directory
[Spectrum Detail]

(RS)-beta-Amino-beta-(4-bromophenyl)propionic acid(39773-47-2)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

39773-47-2(sigmaaldrich)
Hazard InformationBack Directory
[Synthesis]

Malonic acid

141-82-2

4-Bromobenzaldehyde

1122-91-4

(RS)-beta-Amino-beta-(4-bromophenyl)propionic acid

39773-47-2

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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