Ticagrelor Related Compound IV - Names and Identifiers
Name | 2-{[(3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol
|
Synonyms | Ticagrelor InterMediate1 Ticagrelor Related Compound V Ticagrelor Related Compound IV Ticagrelor Related Compound III 2-(6-Amino-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-yloxy)-ethanol 2-[[(3aR,4S,6R,6aS)-6-Aminotetrahydro-2,2-dimethyl-4H-cyclopenta-1,3-dioxol-4-yl]oxy]ethanol 2-((3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yloxy)ethanol Ethanol, 2-[[(3aR,4S,6R,6aS)-6-aminotetrahydro-2,2-dimethyl-4H-cyclopenta-1,3-dioxol-4-yl]oxy]- 2-{[(3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol 2-{[(3Ar,4S,6R,6As)-6-Amino-2,2-Dimethyltetrahydro-3Ah-Cyclopenta[D][1,3]-Dioxol-4-Yl] Oxy}-1-Ethol 2-[[(3aR,4S,6R,6aS)-6-amino-2,2-dimethyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy]ethanol
|
CAS | 274693-55-9
|
EINECS | 1312995-182-4 |
InChI | InChI=1/C10H19NO4/c1-10(2)14-8-6(11)5-7(9(8)15-10)13-4-3-12/h6-9,12H,3-5,11H2,1-2H3/t6-,7+,8+,9-/m1/s1 |
Ticagrelor Related Compound IV - Physico-chemical Properties
Molecular Formula | C10H19NO4
|
Molar Mass | 217.26 |
Density | 1.21 |
Boling Point | 338℃ |
Flash Point | 158℃ |
Vapor Presure | 0mmHg at 25°C |
pKa | 14.33±0.10(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
Refractive Index | 1.52 |
Ticagrelor Related Compound IV - Introduction
2-[[(3aR,4S,6R,6aS)-6-amino-2, [d][1,3]dioxol-4-yl] ethanol is an organic compound, commonly known as cyclopentenyl Oxy ethanol. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: colorless liquid
-molecular formula: C11H19NO4
-Molecular weight: 233.27g/mol
-Melting Point: Uncertain
-Boiling Point: Uncertain
-Solubility: Soluble in water and common organic solvents
Use:
Cyclopentenyl oxyethanol is commonly used in chemical synthesis and organic synthesis reactions, and can be used as a reagent or intermediate. It can also be used as surfactant, dye and drug synthesis.
Method:
Cyclopentenyl oxyethanol can be synthesized by the following steps:
1. The reaction of allyl alcohol and aragonic acid to generate allyl acid.
2. Reaction Allylic acid reacts with excess ammonia in the presence of potassium carbonate to produce an enamide compound.
3. The enamide compound is hydrolyzed under acidic conditions to generate the target product cyclopentenyl oxyethanol.
Safety Information:
Cyclopentenyl oxyethanol is generally safe under correct use and storage, but the following matters still need to be paid attention:
-Avoid contact with skin, eyes and mucous membranes. In case of contact, rinse immediately with plenty of water and seek medical attention.
-Follow laboratory safety practices and use appropriate personal protective equipment, such as lab gloves and goggles.
-Please maintain a well-ventilated laboratory environment when using, avoid inhaling aerosols or vapors.
-This compound may be toxic to aquatic organisms and should avoid pollution to water bodies and the environment.
-When storing, keep it in a dry, cool place, away from fire and oxidizing agents.
Last Update:2024-04-09 02:00:44