-Methyl Gibberellin A4
(1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic acid
CAS: 76784-95-7
Molecular Formula: C9H12O6
-Methyl Gibberellin A4 - Names and Identifiers
| Name | (1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic acid |
| Synonyms | -Cyano Mestanolone -Methyl Gibberellin A4 )-2,17-Dimethylandrostane-3,17-diol (1а,2а,4а)-1,2,4-Cyclohexanetricarboxylic Acid 1,2,4-Cyclohexanetricarboxylicacid, (1a,2a,4a)- (1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic acid (1ALPHA,2ALPHA,4ALPHA)-1,2,4-CYCLOHEXANETRICARBOXYLIC ACID 1,2,4-Cyclohexane tric1,2,4-Cyclohexane tricarboxylic acidarboxylic acid |
| CAS | 76784-95-7 |
| InChI | InChI=1/C9H12O6/c10-7(11)4-1-2-5(8(12)13)6(3-4)9(14)15/h4-6H,1-3H2,(H,10,11)(H,12,13)(H,14,15) |
| InChIKey | WTNDADANUZETTI-NGJCXOISSA-N |
-Methyl Gibberellin A4 - Physico-chemical Properties
| Molecular Formula | C9H12O6 |
| Molar Mass | 216.19 |
| Density | 1.509±0.06 g/cm3 (20 ºC 760 Torr) |
| Melting Point | 182 °C |
| Boling Point | 470.1±45.0 °C(Predicted) |
| Flash Point | 252.2°C |
| Vapor Presure | 3.9E-10mmHg at 25°C |
| pKa | 3.72±0.47(Predicted) |
| Storage Condition | Room Temprature |
| Refractive Index | 1.555 |
-Methyl Gibberellin A4 - Introduction
Nature:
(1alpha,2alpha,4alpha)-1,2, acid is a colorless crystalline solid with a special cyclic structure. It has a melting point of about 182-186 degrees Celsius and is soluble in water and other organic solvents. It is a weak acid that can react with a base in aqueous solution to form the corresponding salt.
Use:
(1alpha,2alpha,4alpha)-1,2, acid has important uses in the field of chemistry. It can be used as a raw material and intermediate in organic synthesis. It can be used to synthesize organic compounds by esterification to generate cyclohexanecarboxylic acid esters. In addition, it can also be used as a ligand in the coordination compound to participate in the coordination reaction of metal ions.
Preparation Method:
(1alpha,2alpha,4alpha)-1,2, acid preparation method can be achieved by the oxidation of cyclohexene. One common method is to react cyclohexene with benzoyl peroxide (benzoyl peroxide) at elevated temperatures. After the reaction, the target product can be obtained by an appropriate purification step.
Safety Information:
(1alpha,2alpha,4alpha)-1,2, acid safety information has not been fully reported, so it needs to be used with caution. Proper laboratory procedures and safety precautions, such as wearing appropriate protective gloves, glasses and laboratory coats, should be observed when using or handling the compound. At the same time, care should be taken to avoid inhaling its dust particles or touching the skin and avoiding swallowing. In case of miscarriage or other accidents, seek medical assistance immediately.
Last Update：2024-04-09 20:52:54
