BOC-D-HIS-OH
N(^a)-Boc-D-histidine
CAS: 50654-94-9
Molecular Formula: C11H17N3O4
BOC-D-HIS-OH - Names and Identifiers
| Name | N(^a)-Boc-D-histidine |
| Synonyms | Boc-D-His-Oh BOC-D-HIS-OH Boc-D-His-OH BOC-D-HISTIDINE Boc-D-histidine N-ALPHA-T-BOC-D-HISTIDINE N-(tert-butoxycarbonyl)-D-histidine N-ALPHA-T-BUTOXYCARBONYL-D-HISTIDINE N-ALPHA-T-BUTYLOXYCARBONYL-D-HISTIDINE NALPHA-(TERT-BUTOXYCARBONYL)-D-HISTIDIN NALPHA-(TERT-BUTOXYCARBONYL)-D-HISTIDINE N-ALPHA-TERT-BUTYLOXYCARBONYL-D-HISTIDINE (2R)-2-[(tert-butoxycarbonyl)amino]-3-(1H-imidazol-5-yl)propanoate |
| CAS | 50654-94-9 |
| InChI | InChI=1/C11H17N3O4/c1-11(2,3)18-10(17)14-8(9(15)16)4-7-5-12-6-13-7/h5-6,8H,4H2,1-3H3,(H,12,13)(H,14,17)(H,15,16)/p-1/t8-/m1/s1 |
BOC-D-HIS-OH - Physico-chemical Properties
| Molecular Formula | C11H17N3O4 |
| Molar Mass | 255.27 |
| Density | 1.275 |
| Melting Point | 193-197 °C |
| Boling Point | 398.5°C (rough estimate) |
| Flash Point | 269.6°C |
| Solubility | DMSO (Slightly), Methanol (Slightly) |
| Vapor Presure | 9.89E-12mmHg at 25°C |
| Appearance | Solid |
| Color | White to Off-White |
| BRN | 4196575 |
| pKa | 3.37±0.10(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.5700 (estimate) |
| MDL | MFCD00037851 |
BOC-D-HIS-OH - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29332900 |
| Hazard Class | IRRITANT |
BOC-D-HIS-OH - Introduction
N(^ a)-Boc-D-histidine(N(α)-Boc-D-histidine) is an organic compound with the following properties:
1. Appearance: N(^ a)-Boc-D-histidine is white crystal or crystalline powder.
2. Solubility: It can be dissolved in water and some organic solvents, such as alcohol and dimethylthionamide.
N(^ a)-Boc-D-histidine has a wide range of applications and uses:
1. chemical synthesis: it is often used as a catalyst and reagent in organic synthesis, involved in the synthesis and modification of peptides, proteins and other organic molecules.
2. Drug research: N(^ a)-Boc-D-histidine is an important amino acid derivative, which can be used in drug research and development, especially in the synthesis and improvement of peptide drugs.
3. biochemical research: it can be used as a substrate, probe and inhibitor in biochemical research, and can be used to study biological processes such as enzyme activity, receptor binding and signal transduction.
N(^ a)-The preparation of Boc-D-histidine usually involves the following steps:
1. First, histidine is obtained by related synthesis methods.
2. Then, using organic synthesis technology, a protecting group (Boc) was introduced into histidine molecule to generate N(^ a)-Boc-D-histidine.
N(^ a)-Boc-D-histidine safety information as follows:
1. Safety evaluation: N(^ a)-The safety of the Boc-D-histidine has not been fully evaluated, so caution is required when using it.
Avoid contact: Avoid direct contact with N(^ a)-Boc-D-histidine, especially to avoid inhalation of its dust or solution.
3. Hazard: N(^ a)-Boc-D-histidine may cause irritation and sensitivity to the eyes, skin and respiratory tract.
4. Personal protection: During contact and operation, it is recommended to wear appropriate personal protective equipment, such as gloves, protective glasses and masks.
When using N(^ a)-Boc-D-histidine, please be sure to refer to its relevant safety data table and follow relevant safety operation specifications in operation.
1. Appearance: N(^ a)-Boc-D-histidine is white crystal or crystalline powder.
2. Solubility: It can be dissolved in water and some organic solvents, such as alcohol and dimethylthionamide.
N(^ a)-Boc-D-histidine has a wide range of applications and uses:
1. chemical synthesis: it is often used as a catalyst and reagent in organic synthesis, involved in the synthesis and modification of peptides, proteins and other organic molecules.
2. Drug research: N(^ a)-Boc-D-histidine is an important amino acid derivative, which can be used in drug research and development, especially in the synthesis and improvement of peptide drugs.
3. biochemical research: it can be used as a substrate, probe and inhibitor in biochemical research, and can be used to study biological processes such as enzyme activity, receptor binding and signal transduction.
N(^ a)-The preparation of Boc-D-histidine usually involves the following steps:
1. First, histidine is obtained by related synthesis methods.
2. Then, using organic synthesis technology, a protecting group (Boc) was introduced into histidine molecule to generate N(^ a)-Boc-D-histidine.
N(^ a)-Boc-D-histidine safety information as follows:
1. Safety evaluation: N(^ a)-The safety of the Boc-D-histidine has not been fully evaluated, so caution is required when using it.
Avoid contact: Avoid direct contact with N(^ a)-Boc-D-histidine, especially to avoid inhalation of its dust or solution.
3. Hazard: N(^ a)-Boc-D-histidine may cause irritation and sensitivity to the eyes, skin and respiratory tract.
4. Personal protection: During contact and operation, it is recommended to wear appropriate personal protective equipment, such as gloves, protective glasses and masks.
When using N(^ a)-Boc-D-histidine, please be sure to refer to its relevant safety data table and follow relevant safety operation specifications in operation.
Last Update：2024-04-09 21:01:54
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