| Identification | Back Directory | [Name]
methyl 4-aminocyclohexane-1-carboxylate | [CAS]
61367-07-5 | [Synonyms]
Nsc145378
methyl 4-aminocyclohexane-1-carboxylate
H-1,4-trans-Achc-OMe·HCl≥ 99% (Titration)
Trans-Methyl 4-aMinocyclohexanecarboxylate HCl
Methyl trans-4-aminocyclohexanecarboxylate, HCl
Methyl 4-aminocyclohexanecarboxylate hydrochloride
trans-4-AMino-cyclohexanecarboxylic acid Methyl ester
trans-Methyl 4-aMinocyclohexanecarboxylate hydrochloride
Methyl trans-4-Aminocyclohexanecarboxylate Hydrochloride
Methyltrans-4-AminocyclohexanecarboxylateHydrochloride>
(1r,4r)-Methyl 4-aMinocyclohexanecarboxylate hydrochloride
trans-1-Amino-4-(methoxycarbonyl)cyclohexane hydrochloride
Methyl trans-4-aminocyclohexane-1-carboxylate hydrochloride
trans-4-AMino-cyclohexanecarboxylic acid Methyl ester hydrochloride
Cyclohexanecarboxylic acid, 4-amino-, methyl ester, hydrochloride, trans-
Cyclohexanecarboxylicacid, 4-aMino-, Methyl ester, hydrochloride (1:1), trans-
(1r,4r)-Methyl 4-(6-(pyrrolidin-1-yl)pyriMidin-4-ylaMino)cyclohexanecarboxylate | [Molecular Formula]
C8H15NO2 | [MDL Number]
MFCD08274538 | [MOL File]
61367-07-5.mol | [Molecular Weight]
193.67 |
| Chemical Properties | Back Directory | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
powder to crystal | [color ]
White to Almost white | [Water Solubility ]
Soluble in water. | [InChI]
InChI=1/C8H15NO2.ClH/c1-11-8(10)6-2-4-7(9)5-3-6;/h6-7H,2-5,9H2,1H3;1H/t6-,7-; | [InChIKey]
NHAYDXCUCXRAMF-MEZFUOHNNA-N | [SMILES]
C([C@@H]1CC[C@@H](N)CC1)(=O)OC.Cl |&1:1,4,r| |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder | [Uses]
Methyl trans-4-aminocyclohexanecarboxylate hydrochloride is generally used as a intermediate in pharmaceutical and chemical research. | [Synthesis]
(Trans)-4-aminocyclohexanecarboxylic acid (200 mg, 1.40 mmol) was suspended in MeOH (5.5 mL) and cooled to -10 ℃. To this was added SOCl2 (204 μL, 2.79 mmol) dropwise, and the mixture was stirred for 15 minutes. The reaction mixture was warmed to ambient temperature for 15 minutes, followed by heating at reflux for 1 hour. After cooling, the mixture was concentrated to afford Methyl trans-4-AMinocyclohexanecarboxylate Hydrochloride (260 mg, 96.1 % yield).
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