Ramelteon Metabolite M-II
- CAS NO.:896736-21-3
- Empirical Formula: C16H21NO3
- Molecular Weight: 275.34
- MDL number: MFCD11977904
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-10-28 16:48:35
What is Ramelteon Metabolite M-II?
Chemical properties
White Solid
The Uses of Ramelteon Metabolite M-II
The major metabolite of Ramelteon in serum (M-II)
The Uses of Ramelteon Metabolite M-II
The major metabolite of Ramelteon in serum (M-II).
What are the applications of Application
Ramelteon Metabolite M-II (mixture of R and S at the hydroxy position) is the major metabolite of ramelteon
Properties of Ramelteon Metabolite M-II
Melting point: | 96-98°C |
Boiling point: | 495.2±45.0 °C(Predicted) |
Density | 1.199±0.06 g/cm3(Predicted) |
storage temp. | Refrigerator |
solubility | Chloroform (Slightly), Methanol (Slightly) |
form | Solid |
pka | 13.42±0.20(Predicted) |
color | White to Off-White |
Safety information for Ramelteon Metabolite M-II
Computed Descriptors for Ramelteon Metabolite M-II
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
(S)-2-(2,6,7,8-tetrahydro-1H-indeno[5,4-b]furan-8-yl)acetic acid
Ramelteon Impurity 10
2-(1,6,7,8-Tetrahydro-2H-indeno[5,4-b]furan-8-yl)ethylaMine hydrochloride
Ramelteon Impurity 22
Despropionyl Ramelteon Hydrochloride
Ramelteon Impurity 6
(R)-2-(2,6,7,8-tetrahydro-1H-indeno[5,4-b]furan-8-yl)acetic acid
(E)-2-(1,6,7,8-Tetrahydro-2H-indeno[5,4-b]furan-8-ylidene)ethylamine
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