emylcamate
- CAS NO.:78-28-4
- Empirical Formula: C7H15NO2
- Molecular Weight: 145.2
- MDL number: MFCD00868182
- EINECS: 2011014
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-10-28 16:48:35
What is emylcamate?
Originator
Striatin,MSD,US,1960
The Uses of emylcamate
Emylcamate is used in combination with compounds that influence brain function and or psychological state to treat herpes virus infection and outbreaks.
Definition
ChEBI: Emylcamate is a carbamate ester.
Manufacturing Process
30.5 g of 3-methyl-3-pentanol, 8.1 g of potassium cyanate and 16.3 g of trichloroacetic acid are heated while stirring at 45°C to 50°C for 24 hours, neutralized by successive addition of anhydrous sodium carbonate. The precipitate is removed from the reaction mixture. Unreacted 3-methyl-3- pentanol is distilled off and the residue is added to a small volume of distilled water. After precipitation and filtration the resulting 3-methyl-3-pentanol carbamate is dried and recrystallized from petroleum ether. MP 54°C to 55°C.
Therapeutic Function
Tranquilizer
Purification Methods
Crystallise the carbamate from 30% aqueous EtOH. [Beilstein 1 IV 1773.]
Properties of emylcamate
Melting point: | 56-58.5° |
Boiling point: | bp1.0 35°; bp0.7 24° |
Density | 0.9441 (estimate) |
refractive index | 1.4206 (estimate) |
pka | 13.54±0.50(Predicted) |
CAS DataBase Reference | 78-28-4 |
Safety information for emylcamate
Computed Descriptors for emylcamate
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
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