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allomethadione

Product Name
allomethadione
CAS No.
526-35-2
Chemical Name
allomethadione
Synonyms
Malazol;Malidone;Aloxidone;Allydione;Alloxidone;allomethadione;3-allyl-5-methyl-oxazolidine-2,4-quinone;5-methyl-3-prop-2-enyl-1,3-oxazolidine-2,4-dione;2,4-Oxazolidinedione, 5-methyl-3-(2-propen-1-yl)-
CBNumber
CB9910067
Molecular Formula
C7H9NO3
Formula Weight
155.15
MOL File
526-35-2.mol
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allomethadione Property

Melting point:
<25 °C
Boiling point:
bp0.5 86-87°; bp1.8 88.90°
Density 
1.3004 (rough estimate)
refractive index 
nD20 1.4710
pka
-2.32±0.40(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CHM0304152
Product name
5-METHYL-3-(PROP-2-EN-1-YL)-1,3-OXAZOLIDINE-2,4-DIONE
Purity
95.00%
Packaging
5MG
Price
$495.86
Updated
2021/12/16
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allomethadione Chemical Properties,Usage,Production

Originator

Aloxidone ,ZYF Pharm Chemical

Definition

ChEBI: Allomethadione is an oxazolidinone.

Manufacturing Process

A mixture of 11.4 parts of 5-methyloxazolidine-2,4-dione and 15 parts anhydrous potassium carbonate in 150 parts of dry acetone is stirred for 0.5 hour. 15 parts of allyl bromide are then added and the mixture boiled under reflux with stirring for 4 hours. After cooling and filtering, the solvent and any unchanged allyl bromide are removed by distillation. The residue is extracted with ether end the extract washed with saturated aqueous sodium bicarbonate until the subsequent water-washings are either neutral or just alkaline to litmus paper. The solvent is then distilled and the residue fractionated when 3- allyl-5-methyloxazolidine-2,4-dione is obtained in 65% yield as a colorless oil, BP: 88°-90°C/1.8 mm, nd20 = 1.4710.
The dry sodium salt of 5-methyloxazolidine-2,4-dione, obtained from 4.6 parts of sodium, 100 parts of ethanol, 12 parts of urea and 23.6 parts of ethyl lactate, is suspended in 100 parts of dry benzene and 30.25 parts of allyl bromide are added. The mixture is boiled under reflux for 20 hours and the benzene decanted or filtered from any solid. The solution is washed with saturated aqueous sodium bicarbonate until the subsequent water-washings are neutral or just alkaline to litmus paper. The dried benzene solution is then distilled to remove solvent and the residue fractionated, when 3-allyl-5- methylosazolidine-2,4-dione is obtained in 27% yield as a colorless oil, BP: 89°-90°C/1 mm, nd20 = 1.4712.
The dry sodium salt of 5-methyloxazolidine-2,4-dione obtained as above is mixed with 100 parts of dry dioxane and 31.25 parts of allyl bromide are added. After boiling under reflex for 24 hours, decanting the solution and distilling off the dioxane under reduced pressure, the residue is dissolved in ether and the ethereal extract mashed with aqueous sodium bicarbonate as above. Fractionation of the residue after removing the olvent furnishes 3-allyl- 5-methyloxazolidine-2,4-dione in 48.5% yield as a colorless oil; BP: 94°- 95°C/11.75 mm; nd20 = 1.4710.

Therapeutic Function

Anticonvulsant, Antiepileptic

allomethadione Preparation Products And Raw materials

Raw materials

Preparation Products

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allomethadione Suppliers

Shaanxi Dideu Medichem Co. Ltd
Tel
029-61856358 15229202216
Fax
029-88380327
Email
1020@dideu.com
Country
China
ProdList
10009
Advantage
58

526-35-2, allomethadione Related Search:


  • Alloxidone
  • Allydione
  • Malazol
  • Malidone
  • 3-allyl-5-methyl-oxazolidine-2,4-quinone
  • 5-methyl-3-prop-2-enyl-1,3-oxazolidine-2,4-dione
  • allomethadione
  • Aloxidone
  • 2,4-Oxazolidinedione, 5-methyl-3-(2-propen-1-yl)-
  • 526-35-2