(2S)-3-{1-[(tert-butoxy)carbonyl]-1H-indol-3-yl}-2-{[(tert-butoxy)carbonyl]amino}propanoic acid
BOC-TRP(BOC)-OH
CAS: 144599-95-1
Molecular Formula: C21H28N2O6
(2S)-3-{1-[(tert-butoxy)carbonyl]-1H-indol-3-yl}-2-{[(tert-butoxy)carbonyl]amino}propanoic acid - Names and Identifiers
(2S)-3-{1-[(tert-butoxy)carbonyl]-1H-indol-3-yl}-2-{[(tert-butoxy)carbonyl]amino}propanoic acid - Physico-chemical Properties
| Molecular Formula | C21H28N2O6 |
| Molar Mass | 404.46 |
| Solubility | Soluble in dimethylformamide (1 mmole in 2 ml). |
| Storage Condition | Sealed in dry,Store in freezer, under -20°C |
| Physical and Chemical Properties | Storage Conditions:-20 ℃ |
(2S)-3-{1-[(tert-butoxy)carbonyl]-1H-indol-3-yl}-2-{[(tert-butoxy)carbonyl]amino}propanoic acid - Introduction
BOC-TRP(BOC)-OH is a chemical compound with the following properties:
1. Appearance: A White to slightly yellow solid powder.
2. Solubility: soluble in common organic solvents, such as dimethyl sulfoxide and dimethylformamide.
3. Stability: Relatively stable at room temperature, but decomposition may occur under high temperature, light or acidic conditions.
BOC-TRP(BOC)-OH is mainly used as a reagent and intermediate in organic synthesis, commonly used in the synthesis of peptides, drugs and bioactive molecules and other compounds.
The preparation method generally uses the following steps for synthesis:
1. First, L-tryptophan reacts with carbon dioxide to generate the N-carboxy acyl group of L-tryptophan.
2. Next, the N-carboxyacyl group obtained in the reaction is reacted with a protecting group reagent such as Boc-OSu to produce the BOC-TRP(BOC)-OH.
Pay attention to safety matters and operating specifications during the preparation process. Wear appropriate protective equipment such as lab gloves, goggles and protective clothing during use. Make sure to work in a well-ventilated area to avoid inhaling gas or dust. Avoid skin contact and accidental ingestion. If you accidentally come into contact with skin or eyes, rinse immediately with plenty of water and seek medical help. In addition, store the substance in a dry, cool, ventilated place, away from fire and oxidizing agents.
1. Appearance: A White to slightly yellow solid powder.
2. Solubility: soluble in common organic solvents, such as dimethyl sulfoxide and dimethylformamide.
3. Stability: Relatively stable at room temperature, but decomposition may occur under high temperature, light or acidic conditions.
BOC-TRP(BOC)-OH is mainly used as a reagent and intermediate in organic synthesis, commonly used in the synthesis of peptides, drugs and bioactive molecules and other compounds.
The preparation method generally uses the following steps for synthesis:
1. First, L-tryptophan reacts with carbon dioxide to generate the N-carboxy acyl group of L-tryptophan.
2. Next, the N-carboxyacyl group obtained in the reaction is reacted with a protecting group reagent such as Boc-OSu to produce the BOC-TRP(BOC)-OH.
Pay attention to safety matters and operating specifications during the preparation process. Wear appropriate protective equipment such as lab gloves, goggles and protective clothing during use. Make sure to work in a well-ventilated area to avoid inhaling gas or dust. Avoid skin contact and accidental ingestion. If you accidentally come into contact with skin or eyes, rinse immediately with plenty of water and seek medical help. In addition, store the substance in a dry, cool, ventilated place, away from fire and oxidizing agents.
Last Update：2024-04-09 20:52:54
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Product Name: Boc-Trp(Boc)-OH Visit Supplier Webpage Request for quotationCAS: 144599-95-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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