(3S)-3-{[(tert-Butoxy)carbonyl]amino}-4-(2,4,5-trifluorophenyl)butanoic acid - Names and Identifiers
Name | Boc-(S)-3-Amino-4-(2,4,5-Trifluorophenyl)-butyric acid
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Synonyms | (S)-Sitagliptin N-Boc-Acid IMpurity Boc-(S)-3-aMino-4-(2,4,5-rifluoro-phenyl)-butyric acid Boc-(S)-3-Amino-4-(2,4,5-Trifluorophenyl)-butyric acid BOC-(S)-3-AMINO-4-(2,4,5-TRIFLUORO-PHENYL)-BUTYRIC ACID (S)-3-(Boc-aMino)-4-(2,4,5-trifluorophenyl)butanoic acid (S)-N-Boc-3-Amino-4-(2,4,5-trifluorophenyl)butanoic acid 3-aMino-5-(tert-butoxy)-5-oxo-4-(2,4,5-trifluorophenyl)pentanoic acid (S)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)butanoic acid (Tert-Butoxy)Carbonyl (S)-3-Amino-4-(2,4,5-trifluoro-phenyl)-butyric acid (3S)-3-{[(tert-Butoxy)carbonyl]amino}-4-(2,4,5-trifluorophenyl)butanoic acid
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CAS | 922178-94-7
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(3S)-3-{[(tert-Butoxy)carbonyl]amino}-4-(2,4,5-trifluorophenyl)butanoic acid - Physico-chemical Properties
Molecular Formula | C15H18F3NO4
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Molar Mass | 333.3 |
Density | 1.292 |
Melting Point | 123 - 125°C |
Boling Point | 443.1±45.0 °C(Predicted) |
Solubility | DMSO (Slightly), Methanol (Slightly) |
Appearance | Solid |
Color | White to Off-White |
pKa | 4.30±0.10(Predicted) |
Storage Condition | 2-8°C |
(3S)-3-{[(tert-Butoxy)carbonyl]amino}-4-(2,4,5-trifluorophenyl)butanoic acid - Introduction
Boc-(S)-3-Amino-4-(2,4,5-Trifluorophenyl)-butyric acid is an organic compound with the following properties:
1. Appearance: White crystalline solid.
2. solubility: can be dissolved in some organic solvents, such as chloroform, ether and dimethylformamide.
3. Melting point: about 80-85°C.
4. Density: about 1.348 g/mL.
5. chemical properties: belongs to a kind of amino acid derivatives containing protecting group.
Boc-(S)-3-Amino-4-(2,4,5-Trifluorophenyl)-butyric acid mainly includes:
1. photosensitizer: in the preparation of photosensitive materials, it can be used as one of the raw materials of photosensitizer.
2. Drug intermediates: intermediates that can be used to synthesize drugs and bioactive molecules.
3. reagent: in the field of organic synthesis and medicine, can be used as the raw material of reagent.
the method for preparing Boc-(S)-3-Amino-4-(2,4,5-Trifluorophenyl)-butyric acid is relatively complicated, and the specific steps are as follows:
1. Add L-glutamyl bromide dropwise to the target compound in an appropriate solution.
2. Add dimethylformamide solution and control the reaction by the corresponding temperature.
3. Add the appropriate amount of alkali to promote the completion of the reaction.
4. Boc-hydrazone was added to form the desired product.
5. Further crystallization and purification were carried out to obtain the final product.
Regarding the safety information of Boc-(S)-3-Amino-4-(2,4,5-Trifluorophenyl)-butyric acid, the following matters need to be noted:
1. The compound may be irritating to the eyes, skin and respiratory system, so it is necessary to wear appropriate protective equipment during operation, such as gloves, glasses and protective masks.
2. Avoid inhaling the dust or gas of the compound. If you inhale it accidentally, you should immediately move to a well-ventilated place and seek medical help if necessary.
3. When using the compound, good laboratory practices should be followed to ensure safety and operability.
Last Update:2024-04-09 21:21:28