114873-08-4
(2S)-2-(tert-butoxycarbonylamino)-3-(5-chloro-1H-indol-3-yl)propanoic acid
CAS: 114873-08-4
Molecular Formula: C16H19ClN2O4
114873-08-4 - Names and Identifiers
| Name | (2S)-2-(tert-butoxycarbonylamino)-3-(5-chloro-1H-indol-3-yl)propanoic acid |
| Synonyms | LogP Boc-L-5-ChloroTryptophan BOC-5-CHLORO-L-TRYPTOPHAN Boc-5-Chloro-L-tryptophan L-N-Boc-5-chlorotryptophan -3-(5-chloro-1H-indol-3-yl) (S)-N-Boc-5-chlorotryptophan N-(tert-Butoxycarbonyl)-5-chloro-L-tryptophan L-Tryptophan, 5-chloro-N-[(1,1-dimethylethoxy)carbonyl]- (2S)-2-(tert-butoxycarbonylamino)-3-(5-chloro-1H-indol-3-yl)propanoic acid (S)-2-(N-(Tert-Butoxy)Carbonyl Amino)-3-(5-chloroindol-3-yl)propanoic acid (S)-2-((tert-Butoxycarbonyl)amino)-3-(5-chloro-1H-indol-3-yl)propanoic acid (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(5-chloro-1H-indol-3-yl)propanoic acid |
| CAS | 114873-08-4 |
| InChI | InChI=1/C16H19ClN2O4/c1-16(2,3)23-15(22)19-13(14(20)21)6-9-8-18-12-5-4-10(17)7-11(9)12/h4-5,7-8,13,18H,6H2,1-3H3,(H,19,22)(H,20,21)/t13-/m0/s1 |
114873-08-4 - Physico-chemical Properties
| Molecular Formula | C16H19ClN2O4 |
| Molar Mass | 338.79 |
| Density | 1.338±0.06 g/cm3(Predicted) |
| Boling Point | 560.8±50.0 °C(Predicted) |
| Flash Point | 292.947°C |
| Vapor Presure | 0mmHg at 25°C |
| pKa | 3.82±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.609 |
114873-08-4 - Introduction
Boc-5-Chloro-L-tryptophan is an organic compound with the following properties:
1. Appearance: Boc-5-chloro-L-tryptophan exists in the form of colorless crystals.
2. Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide (DMSO) and methanol.
The main uses of Boc-5-chlorine-L-tryptophan are as follows:
Chemical synthesis: It is often used as a starting material or intermediate in organic synthesis. It can be used to construct molecular structures with biological activity, such as the synthesis of drugs, pesticides and natural products.
Preparation method of Boc-5-chloro-L-tryptophan:
1. Tryptophan is usually used as a starting material.
2. First, tryptophan is esterified with dimethyl carbonate ((Boc)2O) to obtain Boc-tryptophan.
3. Subsequently, Boc-tryptophan is reacted with chloride (SOCl2) to obtain Boc-5-chloro-L-tryptophan.
Safety Information for Boc-5-Chloro-L-Tryptophan:
1. Boc-5-chlorine-L-tryptophan in the storage and operation process should take appropriate protective measures, such as wearing protective gloves, safety glasses and dust masks.
2. avoid contact with skin, eyes, respiratory system, such as accidental contact, immediately rinse with plenty of water, and seek medical help.
3. storage should be sealed, in a cool, dry place, away from fire and flammable materials.
1. Appearance: Boc-5-chloro-L-tryptophan exists in the form of colorless crystals.
2. Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide (DMSO) and methanol.
The main uses of Boc-5-chlorine-L-tryptophan are as follows:
Chemical synthesis: It is often used as a starting material or intermediate in organic synthesis. It can be used to construct molecular structures with biological activity, such as the synthesis of drugs, pesticides and natural products.
Preparation method of Boc-5-chloro-L-tryptophan:
1. Tryptophan is usually used as a starting material.
2. First, tryptophan is esterified with dimethyl carbonate ((Boc)2O) to obtain Boc-tryptophan.
3. Subsequently, Boc-tryptophan is reacted with chloride (SOCl2) to obtain Boc-5-chloro-L-tryptophan.
Safety Information for Boc-5-Chloro-L-Tryptophan:
1. Boc-5-chlorine-L-tryptophan in the storage and operation process should take appropriate protective measures, such as wearing protective gloves, safety glasses and dust masks.
2. avoid contact with skin, eyes, respiratory system, such as accidental contact, immediately rinse with plenty of water, and seek medical help.
3. storage should be sealed, in a cool, dry place, away from fire and flammable materials.
Last Update：2024-04-10 22:41:56
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