ABP
3-(6-methyl-pyridin-2-ylethynyl)-cyclohex-2-enone-O-methyl-oxime
CAS: 924298-51-1
Molecular Formula: C15H16N2O
ABP - Names and Identifiers
ABP - Physico-chemical Properties
| Molecular Formula | C15H16N2O |
| Molar Mass | 240.3 |
| Density | 1.03±0.1 g/cm3(Predicted) |
| Boling Point | 361.4±52.0 °C(Predicted) |
| pKa | 2.78±0.19(Predicted) |
ABP - Introduction
ABP(3-(6-methylpyridin-2-ylethynyl)-cyclohex-2-enone-O-methyl oxime) is an organic compound. Here is some information about ABP:
Nature:
-Appearance: White solid
-Molecular formula: C14H15N3O
-Molecular weight: 241.29g/mol
-Melting point: about 105-110°C
-Solubility: ABP is soluble in organic solvents such as ethanol, dimethylformamide and dichloromethane.
Use:
ABP is a biologically active molecule commonly used as a research inhibitor or anti-tumor compound. It can be used to explore or inhibit the activity of a variety of enzymes, proteins or cellular processes.
Method:
Although there is no specific preparation method to introduce the synthesis of ABP, the possible synthesis route may include the reaction of 2-chloro-6-methylpyridine and acetylene acetonitrile to prepare pyridoacetylene or ketone group, and further reaction or modification, and then introduce the oxime group. Specific synthetic methods may require detailed access to the relevant chemical literature.
Safety Information:
Due to the lack of specific toxicological data, the safety assessment of ABP is very limited. Therefore, when using ABP, it is necessary to take appropriate laboratory safety measures and follow relevant chemical laboratory practices. Wear appropriate protective equipment, such as laboratory gloves and goggles, if necessary.
Nature:
-Appearance: White solid
-Molecular formula: C14H15N3O
-Molecular weight: 241.29g/mol
-Melting point: about 105-110°C
-Solubility: ABP is soluble in organic solvents such as ethanol, dimethylformamide and dichloromethane.
Use:
ABP is a biologically active molecule commonly used as a research inhibitor or anti-tumor compound. It can be used to explore or inhibit the activity of a variety of enzymes, proteins or cellular processes.
Method:
Although there is no specific preparation method to introduce the synthesis of ABP, the possible synthesis route may include the reaction of 2-chloro-6-methylpyridine and acetylene acetonitrile to prepare pyridoacetylene or ketone group, and further reaction or modification, and then introduce the oxime group. Specific synthetic methods may require detailed access to the relevant chemical literature.
Safety Information:
Due to the lack of specific toxicological data, the safety assessment of ABP is very limited. Therefore, when using ABP, it is necessary to take appropriate laboratory safety measures and follow relevant chemical laboratory practices. Wear appropriate protective equipment, such as laboratory gloves and goggles, if necessary.
Last Update：2024-04-10 22:29:15
