BOC-L-PHE(4-I)
boc-4-iodo-L-phenylalanine
CAS: 62129-44-6
Molecular Formula: C14H18INO4
BOC-L-PHE(4-I) - Names and Identifiers
BOC-L-PHE(4-I) - Physico-chemical Properties
| Molecular Formula | C14H18INO4 |
| Molar Mass | 391.2 |
| Density | 1.560±0.06 g/cm3(Predicted) |
| Melting Point | ~150°C (dec.) |
| Boling Point | 475.3±40.0 °C(Predicted) |
| Specific Rotation(α) | 22.5 º (c=1% in ethyl acetate) |
| Water Solubility | Slightly soluble in water. |
| Appearance | White crystalline powder |
| BRN | 4503851 |
| pKa | 3.84±0.10(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Sensitive | Light Sensitive |
| MDL | MFCD00037119 |
BOC-L-PHE(4-I) - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 8 |
| Hazard Class | IRRITANT |
BOC-L-PHE(4-I) - Introduction
boc-4-iodo-L-phenylalanine is an organic compound with the chemical formula C14H17IN2O4. It is a derivative of hydrazine acid with a protective group Boc and an iodine atom in its molecular structure.
boc-4-iodo-L-phenylalanine peptide synthesis reactions commonly used in organic synthesis, as amino acid derivatives, can be used to synthesize specific positions in the peptide sequence. It can also be used as a raw material for the preparation of other organic compounds, such as drugs, biomarkers, etc.
A common method for preparing boc-4-iodo-L-phenylalanine is by reacting an iodofluoride compound with L-phenylalanine, and then adding a Boc protecting group to the reaction system.
For safety information, boc-4-iodo-L-phenylalanine need to be stored in a low temperature, dry and well ventilated place. Avoid contact with skin, eyes or mouth during use. If exposed to the compound, rinse immediately with plenty of water and seek medical help. Appropriate laboratory safety practices should be followed when handling and handling this compound.
boc-4-iodo-L-phenylalanine peptide synthesis reactions commonly used in organic synthesis, as amino acid derivatives, can be used to synthesize specific positions in the peptide sequence. It can also be used as a raw material for the preparation of other organic compounds, such as drugs, biomarkers, etc.
A common method for preparing boc-4-iodo-L-phenylalanine is by reacting an iodofluoride compound with L-phenylalanine, and then adding a Boc protecting group to the reaction system.
For safety information, boc-4-iodo-L-phenylalanine need to be stored in a low temperature, dry and well ventilated place. Avoid contact with skin, eyes or mouth during use. If exposed to the compound, rinse immediately with plenty of water and seek medical help. Appropriate laboratory safety practices should be followed when handling and handling this compound.
Last Update：2024-04-09 20:02:46
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View History
BOC-L-PHE(4-I)
Thymidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-3-[(2,2-dimethyl-1-oxopropoxy)methyl]- (9CI)
2-(溴甲基)-7-氯苯并[B]噻吩
4-[(三甲基硅烷基)甲基]苯酚
2R,3S)-(+)-3-(苄氧甲基)环氧乙烷-2-甲醇4-硝基苯甲酸酯
1,3-二油酸-2-棕榈酸甘油三酯
六正丁基二锡,六正丁基锡
2-Nonene-6,8-diynamide, N-(2-methylpropyl)-, (2Z)-
1-((3,5-二氯苯基)(苯基)甲基)哌嗪
帕博西尼羟乙基磺酸盐
Thymidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-3-[(2,2-dimethyl-1-oxopropoxy)methyl]- (9CI)
2-(溴甲基)-7-氯苯并[B]噻吩
4-[(三甲基硅烷基)甲基]苯酚
2R,3S)-(+)-3-(苄氧甲基)环氧乙烷-2-甲醇4-硝基苯甲酸酯
1,3-二油酸-2-棕榈酸甘油三酯
六正丁基二锡,六正丁基锡
2-Nonene-6,8-diynamide, N-(2-methylpropyl)-, (2Z)-
1-((3,5-二氯苯基)(苯基)甲基)哌嗪
帕博西尼羟乙基磺酸盐