|
|
| | (S)-(-)-3-CYCLOHEXENECARBOXYLIC ACID Basic information |
| Product Name: | (S)-(-)-3-CYCLOHEXENECARBOXYLIC ACID | | Synonyms: | (S)-(-)-3-CYCLOHEXENECARBOXYLIC ACID;(S)-(?)-1,2,3,6-Tetrahydrobenzoic acid;(1S)-CYCLOHEX-3-ENE-1-CARBOXYLIC ACID(1S)-CYCLOHEX-3-ENE-1-CARBOXYLIC ACID;(1S)-3-Cyclohexene-1-carboxylic acid;(S)-(-)-3-Cyclohexene-1-carboxylic Acid;Chemicalbook(S)-3-Cyclohexene-1-carboxylicAcid;(1S) -3- cyclohexene-1-carboxylate acid;(S)-(-)-3-Cyclohexenecaboxylic acid | | CAS: | 5708-19-0 | | MF: | C7H10O2 | | MW: | 126.15 | | EINECS: | 634-675-3 | | Product Categories: | Edoxaban | | Mol File: | 5708-19-0.mol |  |
| | (S)-(-)-3-CYCLOHEXENECARBOXYLIC ACID Chemical Properties |
| Melting point | 19°C(lit.) | | Boiling point | 118°C/6mmHg(lit.) | | density | 1.126±0.06 g/cm3(Predicted) | | refractive index | 1.4780 to 1.4820 | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | form | clear liquid | | pka | 4.67±0.20(Predicted) | | color | Colorless to Almost colorless | | InChI | InChI=1S/C7H10O2/c8-7(9)6-4-2-1-3-5-6/h1-2,6H,3-5H2,(H,8,9)/t6-/m1/s1 | | InChIKey | VUSWCWPCANWBFG-ZCFIWIBFSA-N | | SMILES | [C@H]1(C(O)=O)CCC=CC1 |
| Hazard Codes | C | | Risk Statements | 34 | | Safety Statements | 26-36/37/39-45 | | RIDADR | UN 3265 8 / PGIII | | HazardClass | 8 | | PackingGroup | III | | HS Code | 2916200090 |
| | (S)-(-)-3-CYCLOHEXENECARBOXYLIC ACID Usage And Synthesis |
| Uses | (S)-3-Cyclohexene-1-carboxylic Acid has been used as a reactant for the preparation of N-[(1R,2S,5S)-2-{[(5-chloroindol-2-yl)carbonyl]amino}-5-(dimethylcarbamoyl)cyclohexyl]-5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxamide hydrochloride, a potent and orally active direct inhibitor of factor Xa. | | Uses | (S)-(-)-3-CYCLOHEXENECARBOXYLIC ACID can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes. | | Synthesis | 54.94 g of cyclohex-3-ene-1(S)-carboxylic acid (R)-(+)-methylbenzylamine salt and 18.2 volumes of H2O were charged to a flask at 20-25°C and stirred. To the mixture obtained further 6.7 volumes of H2O and 10 volumes of EtOAc were added. The mixture obtained was stirred for 15 min, the phases were separated and the organic layer was discarded. The aqueous layer was treated with 10 volumes of MTBE and 2.5 equivalents of 6M HCI were added slowly. The mixture obtained was stirred and two layers were formed, separated and the aqueous layer was extracted with MTBE. The organic layers obtained were combined and washed with aqueous, 30percent NaCl solution. The organic phase obtained was dried over Na2S04, filtered, and from the filtrate obtained solvent was removed in vacuo. Cyclohex-3-ene-1(S)-carboxylic acid in the form of a clear oil was obtained. Yield: 26.13 g (93.3percent of theory). |
| | (S)-(-)-3-CYCLOHEXENECARBOXYLIC ACID Preparation Products And Raw materials |
|