| Identification | Back Directory | [Name]
2-aMino-2-(1H-indol-5-yl)acetic acid | [CAS]
108763-43-5 | [Synonyms]
Amino(1H-indol-5-yl)acetic acid
2-Amino-2-(5-indolyl)acetic acid
1H-Indole-5-acetic acid, α-aMino-
alpha-Amino-1H-indole-5-acetic acid
2-Amino-2-(5-indolyl)aceticacid,98%
Amino(1H-indol-5-yl)acetic acid 95+%
2-(2-Amino-1H-indol-5-yl)acetic acid
2-aMino-2-(1H-indol-5-yl)acetic acid | [Molecular Formula]
C10H10N2O2 | [MDL Number]
MFCD06656882 | [MOL File]
108763-43-5.mol | [Molecular Weight]
190.199 |
| Chemical Properties | Back Directory | [Boiling point ]
438.6±35.0 °C(Predicted) | [density ]
1.422±0.06 g/cm3 (20 ºC 760 Torr) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Powder | [pka]
2.05±0.30(Predicted) | [color ]
Pink |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of α-amino-1H-indole-5-acetic acid from the compound (CAS: 108763-42-4): (f) DL-α-amino-α-(indol-5-yl)acetic acid (6f, 17.3 g, 0.08 mol) was mixed with barium hydroxide (92.12 g, 0.292 mol) in 560 mL of water and stirred at 100°C for The reaction was carried out for 24 h. The reaction process was similar to Example 1d. Upon completion of the reaction, the product α-amino-1H-indole-5-acetic acid was obtained in a yield of 12.1 g (67% yield); the molecular formula was C10H10N2O2-2H2O (molecular weight 226.2). Nuclear magnetic resonance hydrogen spectroscopy (NaOD) data: δ= 4.43 (s, 1H), 6.57 (d, 1H), 7.22 (d, 1H), 7.39 (d, 1H), 7.5 (d, 1H), 7.65 (s, 1H) ppm. | [References]
[1] Patent: US4734407, 1988, A |
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