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1707-14-8

1707-14-8 Structure

1707-14-8 Structure
IdentificationBack Directory
[Name]

PHENMETRAZINE HYDROCHLORIDE CII (200 MG)
[CAS]

1707-14-8
[Synonyms]

marsin
C07433
Mefolin
neo-zine
Preludin
Usaf Ge-1
MFCD00242655
Preludin (TN)
a66hydrochloride
preludinhydrochloride
probese-phydrochloride
WLN: T6M DOTJ B1 CR &GH
phenmetrazinehydrochloride
psychaminea66hydrochloride
VJNXVAVKCZJOFQ-UHFFFAOYSA-N
PHENMETRAZINE METHYLCHLORIDE
Phenmetrazine hydrochloride (USP)
Phenmetrazine Hydrochloride [USAN]
Phenmetrazine hydrochloride solution
3-methyl-2-phenylmorpholinehydrochloride
3-methyl-2-phenyl-morpholinhydrochloride
PHENMETRAZINE HYDROCHLORIDE CII (200 MG)
Ephedrine hydrochloride Solution, 100ppm
Morpholine, 3-methyl-2-phenyl-, hydrochloride
Morpholine, 3-methyl-2-phenyl-, hydrochloride (1:1)
2-phenyl-3-methyltetrahydro-1,4-oxazinehydrochloride
3-methyl-2-phenyltetrahydro-2h-1,4-oxazinehydrochloride
Phenmetrazine HydrochlorideQ: What is Phenmetrazine Hydrochloride Q: What is the CAS Number of Phenmetrazine Hydrochloride Q: What is the storage condition of Phenmetrazine Hydrochloride
[EINECS(EC#)]

216-950-6
[Molecular Formula]

C11H16ClNO
[MOL File]

1707-14-8.mol
[Molecular Weight]

213.704
Chemical PropertiesBack Directory
[Melting point ]

175-177°C
[storage temp. ]

Controlled Substance, -20°C Freezer
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

Anorexic. Controlled substance (stimulant).
[Brand name]

Preludin (Boehringer Ingelheim).
[Originator]

Preludin, Boehringer Ingelheim, US ,1956
[Definition]

ChEBI: Phenmetrazine hydrochloride is an organic molecular entity.
[Manufacturing Process]

10 grams of β-phenyl-α-methyl-β,β'-dihydroxy-diethylamine hydrochloride (produced by hydrogenation in the presence of palladium and charcoal of βphenyl-α-methyl-β-keto-β'-hydroxy-N-benzyl-diethylamine hydrochloride obtained from bromopropiophenone by reacting with benzyl-ethanolamine), are warmed with 10% hydrochloric acid for 6 hours on a water bath.After working up in the usual manner, the hydrochloride of the 2-phenyl-3methyl-morpholine crystallizes out from methanolic hydrochloric acid and acetone, MP = 182°C, according to US Patent 2,835,669.
[Therapeutic Function]

Antiobesity
Safety DataBack Directory
[RIDADR ]

3249
[HazardClass ]

6.1(b)
[PackingGroup ]

III
[Safety Profile]

Poison by ingestion, intravenous, intraperitoneal, and subcutaneous routes. Human reproductive effects. Human teratogenic effects by ingestion: developmental abnormalities of the respiratory and gastrointestinal systems, and effects on newborn including neonatal measures or effects. When heated to decomposition it emits very toxic fumes of NOx and HCl.
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