117048-56-3
17-Acetyl-10,13-dimethyl-6,7,8,10,12,13,14,15octahydro-cyclopenta[a]phenathren-3
CAS: 117048-56-3
Molecular Formula: C21H24O2
117048-56-3 - Names and Identifiers
| Name | 17-Acetyl-10,13-dimethyl-6,7,8,10,12,13,14,15octahydro-cyclopenta[a]phenathren-3 |
| Synonyms | DESOXY TETRA (5ST)Tetraene Methyl DESOXY-TETRAENE(5-ST) Methyl-tetraene Matter PREGAN-1,4,9(11)16-TETRAENE-3,20-DIONE (8ξ,14ξ)-pregna-1,4,9(11),16-tetraene-3,20-dione 17-Acetyl-10,13-dimethyl-6,7,8,10,12,13,14,15octahydro-cyclopenta[a]phenathren-3 17-Acetyl-10,13-dimethyl-6,7,8,10,12,13,14,15-octahydrocyclopenta[a]phenathren-3-one 17-ACETYL-10,13-DIMETHYL-6,7,8,10,12,13,14,15-OCTAHYDRO-CYCLOPENTA[A]PHENANTHREN-3-ONE |
| CAS | 117048-56-3 |
| InChI | InChI=1/C21H24O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h6,8-10,12,16,18H,4-5,7,11H2,1-3H3/t16?,18?,20-,21+/m0/s1 |
117048-56-3 - Physico-chemical Properties
| Molecular Formula | C21H24O2 |
| Molar Mass | 308.41 |
| Density | 1.15±0.1 g/cm3(Predicted) |
| Melting Point | 195-198°C |
| Boling Point | 485.7±45.0 °C(Predicted) |
| Flash Point | 180°C |
| Vapor Presure | 1.38E-09mmHg at 25°C |
| Storage Condition | Refrigerator |
| Refractive Index | 1.59 |
117048-56-3 - Introduction
Tetraengestdione is an organic compound with a specific structure, and its chemical formula is C20H28O2. The following is a brief description of the properties, uses, preparation and safety information of tetraengestdione:
Nature:
-Tetraengestdione is a white to pale yellow crystalline solid with a distinctive odor.
-It has high melting point and stability, insoluble in water, but soluble in organic solvents such as ethanol, ether and acetone.
-This compound can be structurally identified and analyzed by nuclear magnetic resonance (NMR), infrared spectroscopy (IR), mass spectrometry (MS) and other techniques.
Use:
-Tetraengestdione is widely used in the field of medicine and is one of the important intermediates for the synthesis of adrenal cortical hormones.
-It can also be used to synthesize other biologically active compounds, such as steroids.
-In addition, tetraengestdione is also used in research and laboratory reagents.
Preparation Method:
-The main preparation method of tetraengestdione is to synthesize it through multiple steps of chemical synthesis starting from cholesterol.
-This synthesis process includes key steps such as oxidation, ketonization, and ring-closing, and requires appropriate reagents and conditions to proceed.
Safety Information:
-Tetraengestdione is generally stable and safe under normal conditions of use.
-Because it is an organic compound, you should pay attention to protective measures when exposed to tetraene gestadione, such as wearing gloves and goggles.
-During operation, avoid inhaling or ingesting the substance and maintain good ventilation conditions.
-If you accidentally come into contact with or ingest tetraengestdione, you should immediately wash or seek medical help and consult a relevant professional for advice.
Please note that when using tetraengestdione or any chemical substance, you should follow the safety operating procedures and carefully read the safety data sheet and instructions of the relevant chemical substance.
Nature:
-Tetraengestdione is a white to pale yellow crystalline solid with a distinctive odor.
-It has high melting point and stability, insoluble in water, but soluble in organic solvents such as ethanol, ether and acetone.
-This compound can be structurally identified and analyzed by nuclear magnetic resonance (NMR), infrared spectroscopy (IR), mass spectrometry (MS) and other techniques.
Use:
-Tetraengestdione is widely used in the field of medicine and is one of the important intermediates for the synthesis of adrenal cortical hormones.
-It can also be used to synthesize other biologically active compounds, such as steroids.
-In addition, tetraengestdione is also used in research and laboratory reagents.
Preparation Method:
-The main preparation method of tetraengestdione is to synthesize it through multiple steps of chemical synthesis starting from cholesterol.
-This synthesis process includes key steps such as oxidation, ketonization, and ring-closing, and requires appropriate reagents and conditions to proceed.
Safety Information:
-Tetraengestdione is generally stable and safe under normal conditions of use.
-Because it is an organic compound, you should pay attention to protective measures when exposed to tetraene gestadione, such as wearing gloves and goggles.
-During operation, avoid inhaling or ingesting the substance and maintain good ventilation conditions.
-If you accidentally come into contact with or ingest tetraengestdione, you should immediately wash or seek medical help and consult a relevant professional for advice.
Please note that when using tetraengestdione or any chemical substance, you should follow the safety operating procedures and carefully read the safety data sheet and instructions of the relevant chemical substance.
Last Update：2024-04-09 21:04:16
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