4-Amino-2,3-Dihydro-Indole-1-Carboxylic Acid Tert-Butyl Ester
1H-Indole-1-carboxylicacid, 4-amino-2,3-dihydro-, 1,1-dimethylethyl ester
CAS: 885272-42-4
Molecular Formula: C13H18N2O2
4-Amino-2,3-Dihydro-Indole-1-Carboxylic Acid Tert-Butyl Ester - Names and Identifiers
4-Amino-2,3-Dihydro-Indole-1-Carboxylic Acid Tert-Butyl Ester - Physico-chemical Properties
| Molecular Formula | C13H18N2O2 |
| Molar Mass | 234.29 |
| Density | 1.177±0.06 g/cm3(Predicted) |
| Boling Point | 370.4±41.0 °C(Predicted) |
| pKa | 4.19±0.20(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
4-Amino-2,3-Dihydro-Indole-1-Carboxylic Acid Tert-Butyl Ester - Introduction
1H-Indole-1-carboxylicacid, 4-amino-2,3-dihydro-, 1,1-dimethylethyl ester is an organic compound whose chemical formula is C12H14F2N2O2. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: white crystal or solid powder
-Melting point: about 125-127 degrees Celsius
-Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide and dichloromethane
-Stability: Stable at room temperature, but may decompose under strong light
Use:
1H-Indole-1-carboxylicacid, 4-amino-2,3-dihydro-, 1,1-dimethylethyyl ester are commonly used as intermediates in organic synthesis reactions. It can be used to prepare indole compounds, nitrogen-containing compounds and bioactive molecules. In addition, it can also be used for research and development in the field of medicine and pesticides.
Preparation Method:
1H-Indole-1-carboxylicacid, 4-amino-2,3-dihydro-, 1,1-dimethylethyl ester can be obtained by acidification of 4-amino-2, 3-difluoroindole-1-carboxylic acid with tert-butyl alcohol. The reaction is typically carried out under an inert atmosphere with the addition of a suitable catalyst and solvent.
Safety Information:
General laboratory safety practices should be followed when using and handling the compound. It can be irritating to the eyes and skin, so contact should be avoided. Appropriate protective equipment, such as gloves and goggles, should be worn during use. If contact or inhalation occurs, wash the affected area immediately and seek medical help.
Nature:
-Appearance: white crystal or solid powder
-Melting point: about 125-127 degrees Celsius
-Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide and dichloromethane
-Stability: Stable at room temperature, but may decompose under strong light
Use:
1H-Indole-1-carboxylicacid, 4-amino-2,3-dihydro-, 1,1-dimethylethyyl ester are commonly used as intermediates in organic synthesis reactions. It can be used to prepare indole compounds, nitrogen-containing compounds and bioactive molecules. In addition, it can also be used for research and development in the field of medicine and pesticides.
Preparation Method:
1H-Indole-1-carboxylicacid, 4-amino-2,3-dihydro-, 1,1-dimethylethyl ester can be obtained by acidification of 4-amino-2, 3-difluoroindole-1-carboxylic acid with tert-butyl alcohol. The reaction is typically carried out under an inert atmosphere with the addition of a suitable catalyst and solvent.
Safety Information:
General laboratory safety practices should be followed when using and handling the compound. It can be irritating to the eyes and skin, so contact should be avoided. Appropriate protective equipment, such as gloves and goggles, should be worn during use. If contact or inhalation occurs, wash the affected area immediately and seek medical help.
Last Update：2024-04-09 20:49:11
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Product Name: tert-Butyl 4-aminoindoline-1-carboxylate Visit Supplier Webpage Request for quotationCAS: 885272-42-4
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Product Name: 4-AMINO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Visit Supplier Webpage Request for quotation
CAS: 885272-42-4
Tel: 18301782025
Email: 3008007409@qq.com
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CAS: 885272-42-4
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View History
4-Amino-2,3-Dihydro-Indole-1-Carboxylic Acid Tert-Butyl Ester
N,N[(3,6-Dioxo-1,4-cyclohexadiene-1,4-diyl)bis(imino-3,1-propanediyl)]bis[N,N-diethylbenzenemethanaminium]dibromide
1-(Methylamino)-4-[(2-methylphenyl)amino]anthraquinone
POLYFORMALDEHYDE
1-(3H-imidazol-4-ylsulfonyl)-3-piperidinecarboxylic acid
29982-59-0
Kimica Algin K
N-Acetyl-L-alpha-aspartyl-L-alpha-glutamyl-N-[(1S)-1-(carboxymethyl)-3-chloro-2-oxopropyl]-L-valinamide
Benzyl Propionate
ethyl 4-(2,4-dichlorobenzylidene)-2-methyl-1-(4-methylphenyl)-5-oxo-4,5-dihydro-1H-pyrrole-3-carboxylate
N,N[(3,6-Dioxo-1,4-cyclohexadiene-1,4-diyl)bis(imino-3,1-propanediyl)]bis[N,N-diethylbenzenemethanaminium]dibromide
1-(Methylamino)-4-[(2-methylphenyl)amino]anthraquinone
POLYFORMALDEHYDE
1-(3H-imidazol-4-ylsulfonyl)-3-piperidinecarboxylic acid
29982-59-0
Kimica Algin K
N-Acetyl-L-alpha-aspartyl-L-alpha-glutamyl-N-[(1S)-1-(carboxymethyl)-3-chloro-2-oxopropyl]-L-valinamide
Benzyl Propionate
ethyl 4-(2,4-dichlorobenzylidene)-2-methyl-1-(4-methylphenyl)-5-oxo-4,5-dihydro-1H-pyrrole-3-carboxylate