(S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(((benzyloxy)methyl)amino)butanoic acid
(2S)-2-(benzyloxycarbonylamino)-4-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid
CAS: 151132-82-0
Molecular Formula: C27H26N2O6
(S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(((benzyloxy)methyl)amino)butanoic acid - Names and Identifiers
| Name | (2S)-2-(benzyloxycarbonylamino)-4-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid |
| Synonyms | N-Cbz-N'-Fmoc-L-2,4-Diaminobutyric acid N-α-Carbobenzoxy-N-γ-(9-fluorenylmethoxycarbonyl)-L-α,γ-diaminobutyric acid (2S)-2-(benzyloxycarbonylamino)-4-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid (S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(((benzyloxy)methyl)amino)butanoic acid (2S)-2-{[(benzyloxy)carbonyl]amino}-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoic acid (2S)-4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid Butanoic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]-, (2S)- |
| CAS | 151132-82-0 |
| InChI | InChI=1S/C27H26N2O6/c30-25(31)24(29-27(33)34-16-18-8-2-1-3-9-18)14-15-28-26(32)35-17-23-21-12-6-4-10-19(21)20-11-5-7-13-22(20)23/h1-13,23-24H,14-17H2,(H,28,32)(H,29,33)(H,30,31)/t24-/m0/s1 |
(S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(((benzyloxy)methyl)amino)butanoic acid - Physico-chemical Properties
| Molecular Formula | C27H26N2O6 |
| Molar Mass | 474.51 |
| Density | 1.299 |
| Boling Point | 739.8±60.0 °C(Predicted) |
| pKa | 3.86±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD23140994 |
(S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(((benzyloxy)methyl)amino)butanoic acid - Introduction
(2S)-2-(benzyloxycarbonylamino)-4-(benzoic) butanoic acid is also known as Boc-Carboxy-Fmoc-L-2, 4-diaminobutyric acid. Here is some information about the compound:
Properties: Boc-Carboxy-Fmoc-L-2, 4-diaminobutyric acid is a solid powder with a white or off-white appearance. It is stable at room temperature and soluble in some organic solvents, such as dimethyl sulfoxide (DMSO) and chloroform. The compound is relatively stable under acidic conditions and may undergo hydrolysis under alkaline conditions.
Application: Boc-Carboxy-Fmoc-L-2, 4-diaminobutyric acid is usually used as a protecting group in organic synthesis. It can protect the amino group in the amino acid, thereby preventing its non-specific reaction with other reactants. In addition, it is also commonly used in the field of peptide synthesis for the synthesis of peptide chains of specific sequence.
Preparation method: Boc-Carboxy-Fmoc-L-2, 4-diaminobutyric acid is generally obtained by chemical synthesis. The specific preparation method can be carried out using an appropriate chemical synthesis route according to actual needs.
Safety information: During operation, care should be taken to avoid inhalation or contact with the compound. It can cause irritation and damage to the eyes, skin and respiratory system. When in use, wear appropriate personal protective equipment such as gloves, protective glasses and protective face masks. During storage and handling, safe operating procedures should be followed to ensure good ventilation conditions. In the event of contact or misuse, the affected area should be cleaned immediately and medical assistance should be sought.
Properties: Boc-Carboxy-Fmoc-L-2, 4-diaminobutyric acid is a solid powder with a white or off-white appearance. It is stable at room temperature and soluble in some organic solvents, such as dimethyl sulfoxide (DMSO) and chloroform. The compound is relatively stable under acidic conditions and may undergo hydrolysis under alkaline conditions.
Application: Boc-Carboxy-Fmoc-L-2, 4-diaminobutyric acid is usually used as a protecting group in organic synthesis. It can protect the amino group in the amino acid, thereby preventing its non-specific reaction with other reactants. In addition, it is also commonly used in the field of peptide synthesis for the synthesis of peptide chains of specific sequence.
Preparation method: Boc-Carboxy-Fmoc-L-2, 4-diaminobutyric acid is generally obtained by chemical synthesis. The specific preparation method can be carried out using an appropriate chemical synthesis route according to actual needs.
Safety information: During operation, care should be taken to avoid inhalation or contact with the compound. It can cause irritation and damage to the eyes, skin and respiratory system. When in use, wear appropriate personal protective equipment such as gloves, protective glasses and protective face masks. During storage and handling, safe operating procedures should be followed to ensure good ventilation conditions. In the event of contact or misuse, the affected area should be cleaned immediately and medical assistance should be sought.
Last Update：2024-04-09 20:52:54
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