(1S)-1-Amino-1,3,4,5-tetrahydro-3-methyl-2H-3-benzazepin-2-one - Names and Identifiers
Name | (1S)-1-Amino-1,3,4,5-tetrahydro-3-methyl-2H-3-benzazepin-2-one
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Synonyms | 1-aMino-1 (1S)-1-amino-3-methyl-4,5-dihydro-1H-3-benzazepin-2-one (S)-1-amino-3-methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one (1S)-1-Amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on (S)-1-Amino-1,3,4,5-tetrahydro-3-methyl-2H-3-benzazepin-2-one (1S)-1-Amino-1,3,4,5-tetrahydro-3-methyl-2H-3-benzazepin-2-one (1S)-1-Amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one 2H-3-BENZAZEPIN-2-ONE,1-AMINO-1,3,4,5-TETRAHYDRO-3-METHYL-,(1S)- 2H-3-BENZAZEPIN-2-ONE,1-AMINO-1,3,4,5-TETRAHYDRO-3-METHYL-,(1S)-3 2H-3-benzazepin-2-one, 1-amino-1,3,4,5-tetrahydro-3-methyl-, (1S)-
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CAS | 253324-92-4
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InChI | InChI=1/C11H14N2O/c1-13-7-6-8-4-2-3-5-9(8)10(12)11(13)14/h2-5,10H,6-7,12H2,1H3/t10-/m0/s1 |
(1S)-1-Amino-1,3,4,5-tetrahydro-3-methyl-2H-3-benzazepin-2-one - Physico-chemical Properties
Molecular Formula | C11H14N2O
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Molar Mass | 190.24 |
Density | 1.124 |
Melting Point | 98-99 °C |
Boling Point | 372.7±42.0 °C(Predicted) |
Flash Point | 179.2°C |
Vapor Presure | 9.42E-06mmHg at 25°C |
pKa | 7.49±0.20(Predicted) |
Storage Condition | Room Temprature |
Refractive Index | 1.563 |
(1S)-1-Amino-1,3,4,5-tetrahydro-3-methyl-2H-3-benzazepin-2-one - Introduction
(1S)-1-Amino-1,3,4, is an organic compound with the chemical formula C13H16N2O. It is a chiral compound and only one stereoisomer exists. Its molecular structure contains a Benzazepine ring and a ketone group.
This compound has the following properties:
-Appearance: Generally white or light yellow crystalline solid.
-Melting point: About 178-180°C.
-Solubility: Its solubility in water is low, but it has better solubility in some organic solvents such as ethanol and dimethyl sulfoxide.
(1S)-1-Amino-1,3,4, has a wide range of applications:
-Drug Research: It is a representative of a class of aminoketones, which are commonly used in the development of antidepressants.
-Chemical synthesis: It can be used as an intermediate for the synthesis of other organic compounds.
(1S)-1-Amino-1,3,4, 4 can be obtained by chemical synthesis:
A common preparation method is through a series of chemical reactions, such as peroxidation, Nitro reduction, reduction, acyl chloride and aminolysis reactions.
Regarding safety information, due to the low toxicity and danger of the compound, the relevant safety data are limited. However, as a chemical, the following points should be paid attention to when using it:
-Avoid inhalation of dust and contact with skin, eyes and mucous membranes.
-Take appropriate personal protective measures during handling and storage, including wearing gloves, goggles and protective clothing.
-Waste disposal in accordance with local environmental laws and regulations.
Before using and handling the compound, please make sure to read and understand the relevant chemical safety data and operating instructions, and follow the correct laboratory safety operating procedures.
Last Update:2024-04-09 21:04:16