(S)-2-(((9H-fluoren-9-yl)Methoxy)carbonylaMino)pent-4-enoic acid
Fmoc-L-Allylglycine
CAS: 146549-21-5
Molecular Formula: C20H19NO4
(S)-2-(((9H-fluoren-9-yl)Methoxy)carbonylaMino)pent-4-enoic acid - Names and Identifiers
| Name | Fmoc-L-Allylglycine |
| Synonyms | Fmoc-Allyglycine Fmoc-Gly(Allyl)-OH Fmoc-L-Allylglycine FMoc-a-allyl-Gly-OH FMoc-(S)-2-Allylglycine (S)-N-Fmoc-Allylglycine Fmoc-(S)-2-Allylglycine (S)-N-FMOC-Allylglycine FMOC-L-2-allylglycine Hydrochloride FMoc-L-Allyglycine FMoc-L-Allyglycine (S)-2-FMoc-aMino-4-pentenoic acid, FMoc-L-allylglycine (S)-N-(9-Fluorenylmethoxycarbonyl)-2-amino-4-pentenoic acid (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}pent-4-enoate (S)-2-(((9H-fluoren-9-yl)Methoxy)carbonylaMino)pent-4-enoic acid (2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}pent-4-enoic acid (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}pent-4-enoic acid |
| CAS | 146549-21-5 |
| EINECS | 1592732-453-0 |
| InChI | InChI=1/C20H19NO4/c1-2-7-18(19(22)23)21-20(24)25-12-17-15-10-5-3-8-13(15)14-9-4-6-11-16(14)17/h2-6,8-11,17-18H,1,7,12H2,(H,21,24)(H,22,23)/t18-/m1/s1 |
(S)-2-(((9H-fluoren-9-yl)Methoxy)carbonylaMino)pent-4-enoic acid - Physico-chemical Properties
| Molecular Formula | C20H19NO4 |
| Molar Mass | 337.37 |
| Density | 1.2486 (rough estimate) |
| Melting Point | 137.1 °C |
| Boling Point | 473.68°C (rough estimate) |
| Flash Point | 294.3°C |
| Water Solubility | Slightly soluble in water. |
| Solubility | Chloroform (Sparingly), DMSO (Slightly), Methanol (Slightly) |
| Vapor Presure | 1.64E-13mmHg at 25°C |
| Appearance | White powder |
| Color | White to Off-White |
| pKa | 3.72±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.5800 (estimate) |
| MDL | MFCD01311749 |
(S)-2-(((9H-fluoren-9-yl)Methoxy)carbonylaMino)pent-4-enoic acid - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29242990 |
| Hazard Class | IRRITANT |
(S)-2-(((9H-fluoren-9-yl)Methoxy)carbonylaMino)pent-4-enoic acid - Introduction
Fmoc-L-Allylglycine is an amino acid derivative with the following properties:
1. Appearance: colorless to light yellow crystalline powder.
2. Solubility: Soluble in common organic solvents such as dimethyl sulfoxide (DMSO), dichloromethane and methanol.
3. Stability: stable under dry and dark conditions.
Fmoc-L-Allylglycine have the following uses in the synthesis of peptides and proteins:
1. Peptide synthesis: as a peptide synthesis in the use of a protecting group, can protect the amino and carboxyl functional groups of amino acids.
2. Storage stability: As a protecting group in solid-phase synthesis, it can improve the stability of the peptide chain, reduce its degradation and control side reactions.
3. Fluorescent probe: Fmoc-L-Allylglycine can also be used as a fluorescent probe in the study of protein structure and function.
The preparation method of Fmoc-L-Allylglycine is mainly divided into two steps:
1. Synthesis of L-allylglycine: prepared by the reaction of L-glycine and allyl bromide.
2. Fmoc protection: by reacting with N-hydroxybutyrimide ester (Fmoc-OSu), The Fmoc protecting group is introduced into allylglycine.
Fmoc-L-Allylglycine is relatively safe under normal use conditions, the following safety precautions should be paid attention:
1. Experimental operation: in the experimental operation, should avoid contact with the skin, eyes and inhalation of its powder. Wear appropriate protective gloves and eye protection during use.
2. Storage: should be stored in a dry, dark and well ventilated place, away from fire and oxidant.
3. Waste Disposal: Disposal of unused or discarded Fmoc-L-Allylglycine in accordance with local regulations.
1. Appearance: colorless to light yellow crystalline powder.
2. Solubility: Soluble in common organic solvents such as dimethyl sulfoxide (DMSO), dichloromethane and methanol.
3. Stability: stable under dry and dark conditions.
Fmoc-L-Allylglycine have the following uses in the synthesis of peptides and proteins:
1. Peptide synthesis: as a peptide synthesis in the use of a protecting group, can protect the amino and carboxyl functional groups of amino acids.
2. Storage stability: As a protecting group in solid-phase synthesis, it can improve the stability of the peptide chain, reduce its degradation and control side reactions.
3. Fluorescent probe: Fmoc-L-Allylglycine can also be used as a fluorescent probe in the study of protein structure and function.
The preparation method of Fmoc-L-Allylglycine is mainly divided into two steps:
1. Synthesis of L-allylglycine: prepared by the reaction of L-glycine and allyl bromide.
2. Fmoc protection: by reacting with N-hydroxybutyrimide ester (Fmoc-OSu), The Fmoc protecting group is introduced into allylglycine.
Fmoc-L-Allylglycine is relatively safe under normal use conditions, the following safety precautions should be paid attention:
1. Experimental operation: in the experimental operation, should avoid contact with the skin, eyes and inhalation of its powder. Wear appropriate protective gloves and eye protection during use.
2. Storage: should be stored in a dry, dark and well ventilated place, away from fire and oxidant.
3. Waste Disposal: Disposal of unused or discarded Fmoc-L-Allylglycine in accordance with local regulations.
Last Update：2024-04-09 02:00:42
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