Boc-DAP
N(alpha)-boc-L-2,3-diaminopropionic acid
CAS: 73259-81-1
Molecular Formula: C8H16N2O4
Boc-DAP - Names and Identifiers
| Name | N(alpha)-boc-L-2,3-diaminopropionic acid |
| Synonyms | Boc-Dap Boc-Dap-OH Boc-Dapa-OH 3-Amino-Boc-L-alanin N-t-BOC--amino-L-alanine N-Boc-beta-amino-L-alanine Na-Boc-L-2,3-diaminopropionic acid 3-AMINO-(TERT-BUTOXYCARBONYL)-L-ALANINE N(alpha)-boc-L-2,3-diaminopropionic acid 3-amino-N-(tert-butoxycarbonyl)-L-alanine Boc-Dpr-OH, N-Boc-L-2,3-diaminopropanoic acid N-alpha-L-(Butoxycarbonyl)-2,3-diaMinopropionic aci N-alpha-L-(Butoxycarbonyl)-2,3-diaminopropionic acid (2S)-3-amino-2-{[(tert-butoxy)carbonyl]amino}propanoic acid |
| CAS | 73259-81-1 |
| EINECS | 1533716-785-6 |
| InChI | InChI=1/C8H16N2O4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4,9H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1 |
| InChIKey | KRJLRVZLNABMAT-YFKPBYRVSA-N |
Boc-DAP - Physico-chemical Properties
| Molecular Formula | C8H16N2O4 |
| Molar Mass | 204.22 |
| Density | 1.189±0.06 g/cm3(Predicted) |
| Melting Point | 210°C (dec.) |
| Boling Point | 364.4±37.0 °C(Predicted) |
| Specific Rotation(α) | -5.5 º (c=1, acetic acid) |
| Flash Point | 174.2°C |
| Solubility | DMSO (Slightly, Heated, Sonicated), Water (Sparingly, Heated, Sonicated) |
| Vapor Presure | 2.64E-06mmHg at 25°C |
| Appearance | Solid |
| Color | White to Off-White |
| BRN | 4182136 |
| pKa | 2.88±0.16(Predicted) |
| Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
| Refractive Index | 1.488 |
| MDL | MFCD00236843 |
| Use | Reactant for: ? Protein assembly directed by synthetic molecular recognition motifs ? Solid phase synthesis of gramicidin S cyclic analogs with antibiotic and hemolytic activities? Synthesis of HCV protease inhibitor modified analogs ? Solid phase sy |
Boc-DAP - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 10 |
| HS Code | 29241990 |
| Hazard Class | IRRITANT |
Boc-DAP - Introduction
N(alpha)-boc-L-2, 3-diaminoppionic acid, also known as N(alpha)-boc-L-2, 3-diamine propionic acid, is an organic compound. The following is a description of its nature, use, formulation and safety information:
Nature:
-Chemical formula: C9H18N2O4
-Molecular weight: 218.25g/mol
-Appearance: White solid
-Melting point: 75-78°C
-Solubility: Soluble in some organic solvents, such as chloroform and methanol
-Stability: Stable at room temperature
Use:
- N(alpha)-boc-L-2, 3-diaminoppionic acid is a compound with amino acid structure, which has important applications in organic synthesis and medicine.
-It can be used as an intermediate for the synthesis of other compounds, such as the synthesis of polypeptides and drugs.
Preparation Method:
- N(alpha)-boc-L-2, 3-diaminoppionic acid can be synthesized by the following steps:
1. First, L-2, 3-diaminopropionic acid is reacted with tert-butoxycarbonyl (Boc) acylating agent to introduce tert-butoxycarbonyl protecting group under alkaline conditions.
2. Then, the remaining protecting group is removed by acid catalysis to obtain N(alpha)-boc-L-2, 3-diaminoppionic acid.
Safety Information:
- N(alpha)-boc-L-2, the use and handling of 3-diaminoppionic acid should follow laboratory safety procedures.
-When using, avoid inhaling dust or contact with skin and eyes.
-In case of ingestion or contact, wash the affected area immediately and seek medical advice if necessary.
-Take care to store it in a dry, cool place, away from direct sunlight.
Nature:
-Chemical formula: C9H18N2O4
-Molecular weight: 218.25g/mol
-Appearance: White solid
-Melting point: 75-78°C
-Solubility: Soluble in some organic solvents, such as chloroform and methanol
-Stability: Stable at room temperature
Use:
- N(alpha)-boc-L-2, 3-diaminoppionic acid is a compound with amino acid structure, which has important applications in organic synthesis and medicine.
-It can be used as an intermediate for the synthesis of other compounds, such as the synthesis of polypeptides and drugs.
Preparation Method:
- N(alpha)-boc-L-2, 3-diaminoppionic acid can be synthesized by the following steps:
1. First, L-2, 3-diaminopropionic acid is reacted with tert-butoxycarbonyl (Boc) acylating agent to introduce tert-butoxycarbonyl protecting group under alkaline conditions.
2. Then, the remaining protecting group is removed by acid catalysis to obtain N(alpha)-boc-L-2, 3-diaminoppionic acid.
Safety Information:
- N(alpha)-boc-L-2, the use and handling of 3-diaminoppionic acid should follow laboratory safety procedures.
-When using, avoid inhaling dust or contact with skin and eyes.
-In case of ingestion or contact, wash the affected area immediately and seek medical advice if necessary.
-Take care to store it in a dry, cool place, away from direct sunlight.
Last Update：2024-04-09 21:01:54
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Product Name: Boc-L-Dap-OH Request for quotation
CAS: 73259-81-1
Tel: +86-18980427282
Email: hk999@hengkangtech.com
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Email: hk999@hengkangtech.com
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