(S,Z)-5-AMino-2-(dibenzylaMino)-1,6-diphenylhex-4-ene-3-one (DAH-II)
(S,Z)-5-Amino-2-(dibenzylamino)-1,6-diphenylhex-4-en-3-one
CAS: 156732-13-7
Molecular Formula: C32H32N2O
(S,Z)-5-AMino-2-(dibenzylaMino)-1,6-diphenylhex-4-ene-3-one (DAH-II) - Names and Identifiers
| Name | (S,Z)-5-Amino-2-(dibenzylamino)-1,6-diphenylhex-4-en-3-one |
| Synonyms | DAH2 DAH-2 (S)-5-amino-2-(dibenzylamino)-1,6-diphenylhex-4-en-3-one (S,Z)-5-Amino-2-(dibenzylamino)-1,6diphenylhex-4-ene-3-one (S,Z)-5-Amino-2-(dibenzylamino)-1,6-diphenylhex-4-en-3-one (2S,4Z)-5-amino-2-(dibenzylamino)-1,6-diphenylhex-4-en-3-one 2-AMINO-5(S)-N,N-DIBENZYL AMINO-3-OXO-1,6-DIPHENYL HEX-2-ENE (S)-2-AMino-5-(N,N-dibenzylaMino)-4-oxo-1,6-diphenylhex-2-ene (S,Z)-5-AMino-2-(DibenzylaMino)-1,6-Diphenylhex-4-En-3-One (DAH-2) (2S)-5-AMino-2-[bis(phenylMethyl)aMino]-1,6-diphenyl-4-hexen-3-one (S,Z)-5-AMino-2-(dibenzylaMino)-1,6-diphenylhex-4-ene-3-one (DAH-II) (S,Z)-5-Amino-2-(dibenzylamino)-1,6-diphenylhex-4-ene-3-one (DAH-II) 4-Hexen-3-one,5-aMino-2-[bis(phenylMethyl)aMino]-1,6-diphenyl-, (2S)- |
| CAS | 156732-13-7 |
| EINECS | 1312995-182-4 |
| InChI | InChI=1/C32H32N2O/c33-30(21-26-13-5-1-6-14-26)23-32(35)31(22-27-15-7-2-8-16-27)34(24-28-17-9-3-10-18-28)25-29-19-11-4-12-20-29/h1-20,23,31H,21-22,24-25,33H2/b30-23-/t31-/m0/s1 |
(S,Z)-5-AMino-2-(dibenzylaMino)-1,6-diphenylhex-4-ene-3-one (DAH-II) - Physico-chemical Properties
| Molecular Formula | C32H32N2O |
| Molar Mass | 460.61 |
| Density | 1.136±0.06 g/cm3(Predicted) |
| Boling Point | 626.2±55.0 °C(Predicted) |
| Flash Point | 332.49°C |
| Vapor Presure | 0mmHg at 25°C |
| pKa | 5.58±0.70(Predicted) |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.63 |
(S,Z)-5-AMino-2-(dibenzylaMino)-1,6-diphenylhex-4-ene-3-one (DAH-II) - Introduction
(S,Z)-5-Amino-2-(dibenzylamino)-1,6-diphenylhex-4-en-3-one (also known as DABSO) is an organic compound with the formula C20H20N2.
Nature:
DABSO is a solid substance with white to yellowish crystals. It has a high melting point and boiling point, and is non-volatile at room temperature. DABSO is slightly soluble in water and has good solubility in organic solvents. It is a relatively stable compound, but may decompose under light and high temperature conditions.
Use:
DABSO is mainly used as an intermediate in organic synthesis. It can be used in the synthesis of heterocyclic compounds, amino compounds, amine compounds, etc. Due to its double bond and benzene ring structure, DABSO can participate in a variety of chemical reactions and can introduce amino groups into organic molecules.
Method:
The preparation of DABSO is usually accomplished by chemical reaction. One common method of preparation is to substitute two chlorine atoms on the benzene ring with amino groups to form the target compound. The specific synthetic method may vary depending on the experimental conditions and reactants.
Safety Information:
The following safety precautions should be paid attention to when using and storing DABSO: Since DABSO may cause eye and skin irritation, appropriate protective equipment should be worn during operation, such as safety glasses and gloves. In addition, DABSO should also avoid contact with flammable substances and should be stored in a dry, well-ventilated place. When handling DABSO, follow the correct laboratory practices and follow the relevant safe operating instructions. Before using or handling DABSO, it is recommended to consult a chemical expert or refer to the safety data form for more detailed safety information.
Nature:
DABSO is a solid substance with white to yellowish crystals. It has a high melting point and boiling point, and is non-volatile at room temperature. DABSO is slightly soluble in water and has good solubility in organic solvents. It is a relatively stable compound, but may decompose under light and high temperature conditions.
Use:
DABSO is mainly used as an intermediate in organic synthesis. It can be used in the synthesis of heterocyclic compounds, amino compounds, amine compounds, etc. Due to its double bond and benzene ring structure, DABSO can participate in a variety of chemical reactions and can introduce amino groups into organic molecules.
Method:
The preparation of DABSO is usually accomplished by chemical reaction. One common method of preparation is to substitute two chlorine atoms on the benzene ring with amino groups to form the target compound. The specific synthetic method may vary depending on the experimental conditions and reactants.
Safety Information:
The following safety precautions should be paid attention to when using and storing DABSO: Since DABSO may cause eye and skin irritation, appropriate protective equipment should be worn during operation, such as safety glasses and gloves. In addition, DABSO should also avoid contact with flammable substances and should be stored in a dry, well-ventilated place. When handling DABSO, follow the correct laboratory practices and follow the relevant safe operating instructions. Before using or handling DABSO, it is recommended to consult a chemical expert or refer to the safety data form for more detailed safety information.
Last Update：2024-04-10 22:29:15
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