Nɑ-芴甲氧羰基-N-in-叔丁氧羰基-L-色氨酸五氟苯酯
FMOC-TRP(BOC)-OPFP
CAS: 181311-44-4
Molecular Formula: C37H29F5N2O6
Nɑ-芴甲氧羰基-N-in-叔丁氧羰基-L-色氨酸五氟苯酯 - Names and Identifiers
Nɑ-芴甲氧羰基-N-in-叔丁氧羰基-L-色氨酸五氟苯酯 - Physico-chemical Properties
| Molecular Formula | C37H29F5N2O6 |
| Molar Mass | 692.63 |
| Storage Condition | Store at 0°C |
| Physical and Chemical Properties | Storage Conditions: Store at 0 ℃ |
Nɑ-芴甲氧羰基-N-in-叔丁氧羰基-L-色氨酸五氟苯酯 - Introduction
FMOC-TRP(BOC)-OPFP is an organic compound with the molecular formula C35H30F5NO6. The following is a description of the properties, uses, preparation and safety information of this compound:
Properties: FMOC-TRP(BOC)-OPFP is a white crystalline solid with good solubility. It is a strongly acidic compound and can be hydrolyzed rapidly. Soluble in chloroform, acetonitrile and dichloromethane, but insoluble in water.
use: The compound is commonly used in organic synthesis as a protecting group or active compound. It can be used as a protecting group for alanine esters and tyrosine esters of amino acids. In addition, it can also be used in steroid synthesis and biomedical research.
Preparation method: The preparation method of FMOC-TRP(BOC)-OPFP is complicated. In general, it is obtained by reacting fluorenecyl chloride, tert-butoxycarbonyl tryptophan and pentafluorophenic acid through an organic synthesis method.
SAFETY INFORMATION: Due to the strong acidity and potential hydrolysis properties of this compound, precautions should be taken when using it. Avoid contact with skin and eyes, and make sure to operate in a well-ventilated environment. When storing and handling the compound, the relevant safety procedures should be followed.
Properties: FMOC-TRP(BOC)-OPFP is a white crystalline solid with good solubility. It is a strongly acidic compound and can be hydrolyzed rapidly. Soluble in chloroform, acetonitrile and dichloromethane, but insoluble in water.
use: The compound is commonly used in organic synthesis as a protecting group or active compound. It can be used as a protecting group for alanine esters and tyrosine esters of amino acids. In addition, it can also be used in steroid synthesis and biomedical research.
Preparation method: The preparation method of FMOC-TRP(BOC)-OPFP is complicated. In general, it is obtained by reacting fluorenecyl chloride, tert-butoxycarbonyl tryptophan and pentafluorophenic acid through an organic synthesis method.
SAFETY INFORMATION: Due to the strong acidity and potential hydrolysis properties of this compound, precautions should be taken when using it. Avoid contact with skin and eyes, and make sure to operate in a well-ventilated environment. When storing and handling the compound, the relevant safety procedures should be followed.
Last Update：2024-04-10 22:29:15
