| Company Name: |
LGC Science (Shanghai) Ltd.
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| Tel: |
17717235263 |
| Email: |
cindy.yang@lgcgroup.com |
| Products Intro: |
Product Name:Fenbutrazate
CAS:4378-36-3
Purity:具体纯度，见COA Package:100mg Remarks:TRC-F247250
|
| Company Name: |
CLEARSYNTH LABS LTD.
|
| Tel: |
+91-22-45045900 |
| Email: |
sales@clearsynth.com |
| Products Intro: |
Product Name:Fenbutrazate
CAS:4378-36-3
|
| Company Name: |
United States Biological
|
| Tel: |
800.520.3011 or 781.639.5092 |
| Email: |
chemicals@usbio.net |
| Products Intro: |
Product Name:Fenbutrazate
CAS:4378-36-3
|
|
| | fenbutrazate Basic information |
| Product Name: | fenbutrazate | | Synonyms: | 2-Phenylbutyric acid 2-(3-methyl-2-phenylmorpholino)ethyl ester;Fenbutrazatum;Phenbutrazatum;2-(3-methyl-2-phenyl-morpholin-4-yl)ethyl 2-phenylbutanoate;2-(3-methyl-2-phenylmorpholin-4-yl)ethyl 2-phenylbutanoate;2-phenylbutyric acid 2-(3-methyl-2-phenyl-morpholin-4-yl)ethyl ester;2-(3-Methyl-2-phenylMorpholino)ethyl 2-Phenylbutyrate;α-Ethylbenzeneacetic Acid 2-(3-Methyl-2-phenyl-4-Morpholinyl)ethyl Ester | | CAS: | 4378-36-3 | | MF: | C23H29NO3 | | MW: | 367.48 | | EINECS: | 224-480-8 | | Product Categories: | Aromatics;Heterocycles;Intermediates & Fine Chemicals;Neurochemicals;Pharmaceuticals | | Mol File: | 4378-36-3.mol |  |
| | fenbutrazate Chemical Properties |
| Boiling point | bp0.05 235-240° | | solubility | Chloroform (Slightly), Dichloromethane (Slightly), DMSO (Slightly), Methanol (Slightly) | | form | Oil to Thick Oil | | color | Pale Yellow to Very Dark Orange |
| | fenbutrazate Usage And Synthesis |
| Originator | Phenbutrazate,Shanghai Lansheng | | Uses | Fenbutrazate is a derivative of Phenmetrazine (P314500). Fenbutrazate is a psychostimulant used as an anorexigen (appetite suppressant). | | Definition | ChEBI: Fenbutrazate is a member of morpholines. | | Manufacturing Process | 1105 g of 2-phenyl-3-methyl-4-(α-hydroxyethyl)-tetrahydro-1,4-oxazine-(4-
(2-hydroxyethyl)-3-methyl-2-phenylmorphotine) are dissolved in 4000 ml of
anhydrous toluene. 910 g of α-phenyl-α-ethyl acetic acid chloride (2-ethyl-2-
phenyl-acetylchloride) are dissolved in 400 ml of anhydrous toluene and the
resulting solution is slowly added to the heated solution of the tetrahydro-1,4-
oxazine compound. The mixture is then heated to boiling for about 5 hours.
About 1000 g of ice are added to the cooled reaction mixture, which is then
rendered alkaline by the addition of 20% sodium carbonate solution to a pH of
9.0. Thereafter the mixture is vigorously stirred by means of a turbine mixer
for one hour and the toluene phase is separated. The toluene solution is
washed with 1000 ml of saturated sodium chloride solution and is dried over
anhydrous sodium sulfate. The toluene is then evaporated and the residue is
subjected to high vacuum distillation. 1650 g of α-phenyl-α-ethylacetic acid
(2-phenyl-3-methyltetrahydro-1,4-oxazine)-N-ethyl ester (fenburazate),
boiling at 235°-240°C/0.05 mm are obtained thereby in a yield of 90.5% of
the theoretical yield. | | Therapeutic Function | Anorexic, Central stimulant | | Synthesis | Phenbutrazate is prepared by condensing Nhydroxyethylphenmetrazine
(R = CH2CH2OH)
with 2-phenylbutyric acid. The N-hydroxyethyl
compound is obtained in the same manner as
phendimetrazine . |
| | fenbutrazate Preparation Products And Raw materials |
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