5-AMINO-1-BOC-2,3-DIHYDROINDOLE
1-BOC-5-AMINO-2,3-DIHYDRO-INDOLE
CAS: 129487-92-9
Molecular Formula: C13H18N2O2
5-AMINO-1-BOC-2,3-DIHYDROINDOLE - Names and Identifiers
5-AMINO-1-BOC-2,3-DIHYDROINDOLE - Physico-chemical Properties
| Molecular Formula | C13H18N2O2 |
| Molar Mass | 234.29 |
| Density | 1.177±0.06 g/cm3(Predicted) |
| Boling Point | 385.2±41.0 °C(Predicted) |
| pKa | 5.44±0.20(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
5-AMINO-1-BOC-2,3-DIHYDROINDOLE - Risk and Safety
| Hazard Class | IRRITANT |
5-AMINO-1-BOC-2,3-DIHYDROINDOLE - Introduction
1-BOC-5-amino-2, 3-indoline is an organic compound with a tert-butyl carbonate protecting group (BOC) and an amino functional group in its molecular structure. The following is a description of its nature, use, formulation and safety information:
Nature:
1-BOC-5-amino-2, 3-indoline is a solid, white crystal or crystalline powder at room temperature. It is soluble in some organic solvents, such as methanol and propylene glycol, while the solubility in water is low. It has thermal stability and chemical stability, and can undergo chemical reactions under certain conditions.
Use:
1-BOC-5-amino -2, 3-indoline is mainly used in the field of organic synthesis. It can be used as an intermediate for the synthesis of other compounds, especially in the synthesis of drugs. It is a common amino protecting group that can protect the amino group during the synthesis to prevent unwanted reactions. When necessary, the protecting group can be removed by appropriate reaction conditions to obtain the desired amino compound.
Preparation Method:
1-BOC-5-amino-2, 3-indoline is generally obtained by chemical synthesis. A common preparation method is by the reaction of 2,3-indoline and tert-butyl bromoacetate to give 1-BOC-5-amino-2, 3-indoline.
Safety Information:
1-BOC-5-amino -2, 3-indoline has certain safety under conventional conditions. However, when handling this compound, care should be taken to follow laboratory safety procedures and wear appropriate personal protective equipment, such as laboratory gloves and protective glasses. In addition, it should be stored in a dry, cool, well-ventilated place, away from fire and oxidants. If ingestion or contact with skin or eyes, seek medical attention immediately and obtain professional first aid.
Nature:
1-BOC-5-amino-2, 3-indoline is a solid, white crystal or crystalline powder at room temperature. It is soluble in some organic solvents, such as methanol and propylene glycol, while the solubility in water is low. It has thermal stability and chemical stability, and can undergo chemical reactions under certain conditions.
Use:
1-BOC-5-amino -2, 3-indoline is mainly used in the field of organic synthesis. It can be used as an intermediate for the synthesis of other compounds, especially in the synthesis of drugs. It is a common amino protecting group that can protect the amino group during the synthesis to prevent unwanted reactions. When necessary, the protecting group can be removed by appropriate reaction conditions to obtain the desired amino compound.
Preparation Method:
1-BOC-5-amino-2, 3-indoline is generally obtained by chemical synthesis. A common preparation method is by the reaction of 2,3-indoline and tert-butyl bromoacetate to give 1-BOC-5-amino-2, 3-indoline.
Safety Information:
1-BOC-5-amino -2, 3-indoline has certain safety under conventional conditions. However, when handling this compound, care should be taken to follow laboratory safety procedures and wear appropriate personal protective equipment, such as laboratory gloves and protective glasses. In addition, it should be stored in a dry, cool, well-ventilated place, away from fire and oxidants. If ingestion or contact with skin or eyes, seek medical attention immediately and obtain professional first aid.
Last Update：2024-04-09 20:52:54
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View History
5-AMINO-1-BOC-2,3-DIHYDROINDOLE
(p-chloro-o-methylphenoxy)acetic acid, compound with methylamine (1:1)
3-[(4-甲基哌嗪-1-基)甲基]苯胺
Anhydro Galanthamine
4-羟基-6-甲氧基喹啉-3-羧酸乙酯
Tetranbutylammoniumhydroxidesolninmethanol
2-氨基-2-甲基丙酸甲酯
2-((3-PHENOXYPHENYL)METHYLENE)INDANE-1,3-DIONE
利福霉素S
反式-2-((4-正丙基)环己基)-1,3-丙二醇
(p-chloro-o-methylphenoxy)acetic acid, compound with methylamine (1:1)
3-[(4-甲基哌嗪-1-基)甲基]苯胺
Anhydro Galanthamine
4-羟基-6-甲氧基喹啉-3-羧酸乙酯
Tetranbutylammoniumhydroxidesolninmethanol
2-氨基-2-甲基丙酸甲酯
2-((3-PHENOXYPHENYL)METHYLENE)INDANE-1,3-DIONE
利福霉素S
反式-2-((4-正丙基)环己基)-1,3-丙二醇