Boc-Trp(CHO)-OH
N(alpha)-boc-N(in)-formyl-L-tryptophan
CAS: 47355-10-2
Molecular Formula: C17H20N2O5
Boc-Trp(CHO)-OH - Names and Identifiers
| Name | N(alpha)-boc-N(in)-formyl-L-tryptophan |
| Synonyms | BOC-TRP(CHO) Boc-Trp(For)-OH BOC-TRP(FOR)-OH BOC-TRP(CHO)-OH Boc-Trp(CHO)-OH BOC-L-TRP(FOR)-OH BOC-L-TRP(FORMYL)-OH BOC-NIN-FORMYL-L-TRYPTOPHAN BOC-L-TRYPTOPHAN(NIN-FORMYL) Boc-L-Trp(Formyl)-OH.solvent N-α-Boc-N-in-formyl-L-tryptophan na-T-boc-N-in-formyl-L-tryptophan N(alpha)-boc-N(in)-formyl-L-tryptophan N-(tert-butoxycarbonyl)-1-formyl-L-tryptophan N-alpha-t-butyloxycabonyl-N-formyl-L-tryptophane N alpha-(tert-Butoxycarbonyl)-N1-formyl-L-tryptophan |
| CAS | 47355-10-2 |
| InChI | InChI=1/C17H20N2O5/c1-17(2,3)24-16(23)18-13(15(21)22)8-11-9-19(10-20)14-7-5-4-6-12(11)14/h4-7,9-10,13H,8H2,1-3H3,(H,18,23)(H,21,22)/t13-/m0/s1 |
Boc-Trp(CHO)-OH - Physico-chemical Properties
| Molecular Formula | C17H20N2O5 |
| Molar Mass | 332.35 |
| Density | 1.26±0.1 g/cm3(Predicted) |
| Melting Point | ~100°C (dec.) |
| Appearance | Crystalline powder |
| Color | White to off-white |
| BRN | 4299614 |
| pKa | 3.82±0.10(Predicted) |
| Storage Condition | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
| Sensitive | Light Sensitive |
| Refractive Index | 1.58 |
| MDL | MFCD00065992 |
Boc-Trp(CHO)-OH - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 8 |
| HS Code | 2933 99 80 |
Boc-Trp(CHO)-OH - Introduction
N(alpha)-boc-N(in)-formyl-L-tryptophan is an organic compound with the chemical formula C20H22N2O4. It is a derivative of tryptophan, prepared by introducing tert-butoxycarbonyl and aldehyde groups on the tryptophan molecule.
N(alpha)-boc-N(in)-formyl-L-tryptophan have some of the following properties:
-Appearance is white crystalline solid or solid powder;
-Relatively stable at room temperature, soluble in some organic solvents such as chloroform, dimethylformamide and ethanol;
-Under acidic conditions, partial hydrolysis may occur.
The main uses of N(alpha)-boc-N(in)-formyl-L-tryptophan are as follows:
-In organic synthesis, it can be used as an indirect amino acid protecting group for the synthesis of biologically active peptide compounds;
-as an intermediate in research and production, for the synthesis of drugs, medical diagnostic reagents and biological materials;
-In biochemistry and biotechnology research, it can be used to study enzyme catalytic reactions, protein structure and its mechanism of action.
N(alpha)-boc-N(in)-formyl-L-tryptophan are generally prepared by chemical synthesis. Specific steps involve the introduction of a tert-butoxycarbonyl group and an aldehyde group on the tryptophan molecule.
Regarding safety information, under correct handling and storage conditions, N(alpha)-boc-N(in)-formyl-L-tryptophan are relatively safe compounds. However, due to its chemical properties and potential irritation, it is still recommended to take appropriate safety measures when using it, such as wearing protective gloves, glasses and laboratory coats to ensure a well-ventilated working environment. Avoid skin contact and inhalation during operation. In case of contact with skin or eyes, rinse immediately with plenty of water and seek medical help.
N(alpha)-boc-N(in)-formyl-L-tryptophan have some of the following properties:
-Appearance is white crystalline solid or solid powder;
-Relatively stable at room temperature, soluble in some organic solvents such as chloroform, dimethylformamide and ethanol;
-Under acidic conditions, partial hydrolysis may occur.
The main uses of N(alpha)-boc-N(in)-formyl-L-tryptophan are as follows:
-In organic synthesis, it can be used as an indirect amino acid protecting group for the synthesis of biologically active peptide compounds;
-as an intermediate in research and production, for the synthesis of drugs, medical diagnostic reagents and biological materials;
-In biochemistry and biotechnology research, it can be used to study enzyme catalytic reactions, protein structure and its mechanism of action.
N(alpha)-boc-N(in)-formyl-L-tryptophan are generally prepared by chemical synthesis. Specific steps involve the introduction of a tert-butoxycarbonyl group and an aldehyde group on the tryptophan molecule.
Regarding safety information, under correct handling and storage conditions, N(alpha)-boc-N(in)-formyl-L-tryptophan are relatively safe compounds. However, due to its chemical properties and potential irritation, it is still recommended to take appropriate safety measures when using it, such as wearing protective gloves, glasses and laboratory coats to ensure a well-ventilated working environment. Avoid skin contact and inhalation during operation. In case of contact with skin or eyes, rinse immediately with plenty of water and seek medical help.
Last Update：2024-04-09 20:02:46
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CAS: 47355-10-2
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Mobile: 18021002903
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