N-芴甲氧羰基-D-高瓜氨酸
Fmoc-D-Homocit-OH
CAS: 201485-38-3
Molecular Formula: C22H25N3O5
N-芴甲氧羰基-D-高瓜氨酸 - Names and Identifiers
N-芴甲氧羰基-D-高瓜氨酸 - Physico-chemical Properties
| Molecular Formula | C22H25N3O5 |
| Molar Mass | 411.45 |
| Density | 1.292±0.06 g/cm3(Predicted) |
| Boling Point | 676.0±55.0 °C(Predicted) |
| pKa | 3.89±0.21(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
N-芴甲氧羰基-D-高瓜氨酸 - Introduction
Fmoc-D-Homocit-OH is an amino acid derivative with specific properties and applications. The following is an introduction to its nature, use, preparation and safety information:
1. Nature:
-chemical name: N-[(9h-hydrofuran [3,2,1-ij] quinolin-1-yl) formyl]-D-high citrulline
-Molecular formula: C27H24N2O6
-Molecular Weight: 472.49
-Appearance: White solid
-Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide, dichloromethane, etc.
2. Use:
-Biochemistry: Fmoc-D-Homocit-OH can be used to synthesize specific amino acids in peptides or proteins to study their biological activity, structure and function.
-Drug development: Fmoc-D-Homocit-OH can be used as an important intermediate in drug synthesis for the synthesis of biologically active molecules.
-Chemical synthesis: As a kind of chiral amino acid, Fmoc-D-Homocit-OH can be used in Chiral synthesis reactions.
3. Preparation method:
Fmoc-D-Homocit-OH are prepared by a variety of methods, usually by chemical synthesis. Detailed synthetic routes can be found in the relevant literature or patents.
4. Safety Information:
- Fmoc-D-Homocit-OH should be kept away from fire and oxidant, and keep sealed to avoid moisture.
-In use should wear protective glasses and protective gloves, avoid contact with the skin and inhalation of its dust.
-For accidental contact, rinse immediately with plenty of water and seek medical help.
-When used in the laboratory, the relevant safety procedures and operating guidelines should be followed.
1. Nature:
-chemical name: N-[(9h-hydrofuran [3,2,1-ij] quinolin-1-yl) formyl]-D-high citrulline
-Molecular formula: C27H24N2O6
-Molecular Weight: 472.49
-Appearance: White solid
-Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide, dichloromethane, etc.
2. Use:
-Biochemistry: Fmoc-D-Homocit-OH can be used to synthesize specific amino acids in peptides or proteins to study their biological activity, structure and function.
-Drug development: Fmoc-D-Homocit-OH can be used as an important intermediate in drug synthesis for the synthesis of biologically active molecules.
-Chemical synthesis: As a kind of chiral amino acid, Fmoc-D-Homocit-OH can be used in Chiral synthesis reactions.
3. Preparation method:
Fmoc-D-Homocit-OH are prepared by a variety of methods, usually by chemical synthesis. Detailed synthetic routes can be found in the relevant literature or patents.
4. Safety Information:
- Fmoc-D-Homocit-OH should be kept away from fire and oxidant, and keep sealed to avoid moisture.
-In use should wear protective glasses and protective gloves, avoid contact with the skin and inhalation of its dust.
-For accidental contact, rinse immediately with plenty of water and seek medical help.
-When used in the laboratory, the relevant safety procedures and operating guidelines should be followed.
Last Update：2024-04-09 15:17:54
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View History
N-芴甲氧羰基-D-高瓜氨酸
N-{4-[(2,4,6-trimethylphenyl)sulfamoyl]phenyl}propanamide
Methanone, (2-chloro-5-hydroxyphenyl)-1-pyrrolidinyl-
1-(2-hydroxy-5-tert-nonylphenyl)ethan-1-one oxime
ALPHA-甲基-3,5-二(三氟甲基)苄醇
Sorafenib tosylate
BOC-环丙基甘氨酸
Tris[2-(6-methyl-5-phenyl-2-pyridinyl)phenyl]-iridium
2-METHYL-1H-INDOLE-3-CARBOXYLIC ACID
1-PROPYL-1H-PYRAZOL-4-YLBORONIC ACID
N-{4-[(2,4,6-trimethylphenyl)sulfamoyl]phenyl}propanamide
Methanone, (2-chloro-5-hydroxyphenyl)-1-pyrrolidinyl-
1-(2-hydroxy-5-tert-nonylphenyl)ethan-1-one oxime
ALPHA-甲基-3,5-二(三氟甲基)苄醇
Sorafenib tosylate
BOC-环丙基甘氨酸
Tris[2-(6-methyl-5-phenyl-2-pyridinyl)phenyl]-iridium
2-METHYL-1H-INDOLE-3-CARBOXYLIC ACID
1-PROPYL-1H-PYRAZOL-4-YLBORONIC ACID