- D-2-Abu-Ome.Hcl
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2026-08-07
- CAS:85774-09-0
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1T+
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| | METHYL D-HOMOALANINATE HCL Basic information |
| Product Name: | METHYL D-HOMOALANINATE HCL | | Synonyms: | METHYL D-HOMOALANINATE HCL;Methyl D-homoalaninate hydrochloride;Butanoic acid, 2-aMino-, Methyl ester, hydrochloride (1:1), (2R)-;D-alpha-Aminobutyric acid methyl ester hydrochloride;Butanoic acid, 2-aMino-, Methyl ester, hydrochloride , (2R)-;Methyl (R)-2-aminobutyrate HCL;(R)-2-AMino-butyric acid Methyl ester;(R)-methyl 2-aminobutanoate hydrochloride | | CAS: | 85774-09-0 | | MF: | C5H11NO2.ClH | | MW: | 153.61 | | EINECS: | 675-786-7 | | Product Categories: | | | Mol File: | 85774-09-0.mol |  |
| | METHYL D-HOMOALANINATE HCL Chemical Properties |
| Melting point | 124-126 °C | | storage temp. | Inert atmosphere,Room Temperature | | Appearance | White to off-white Solid | | Optical Rotation | Consistent with structure | | InChI | InChI=1/C5H11NO2.ClH/c1-3-4(6)5(7)8-2;/h4H,3,6H2,1-2H3;1H/t4-;/s3 | | InChIKey | AHAQQEGUPULIOZ-NDILARRWNA-N | | SMILES | [C@@H](N)(CC)C(=O)OC.Cl |&1:0,r| |
| | METHYL D-HOMOALANINATE HCL Usage And Synthesis |
| Uses | (R)-2-Aminobutanoic Acid Methyl Ester Hydrochloride is used as a reagent in the synthesis of pteridine derivatives which have antibacterial and antifungal activies. (R)-2-Aminobutanoic Acid Methyl Ester Hydrochloride is also used in the synthesis of diazepanones as dipeptidyl peptidase IV inhibitors. | | Synthesis | The general procedure for the synthesis of DL-2-aminobutyric acid methyl ester hydrochloride from methanol and Boc-L-2-aminobutyric acid was as follows: 10.0 g (49.2 mmol) of Boc-L-2-aminobutyric acid was dissolved in 100 mL of methanol, and 6 mL (82.2 mmol) of thionyl chloride was added slowly and dropwise at 0 °C. The reaction mixture was stirred at room temperature for 14 h before the solvent was removed by vacuum evaporation. Finally, 7.6 g (101% yield) of DL-2-aminobutyric acid methyl ester hydrochloride was obtained, whose mass spectrometry analysis showed that the (M + H)+ peak was located at 118 m/z. | | References | [1] Patent: US2010/144681, 2010, A1. Location in patent: Page/Page column 67 |
| | METHYL D-HOMOALANINATE HCL Preparation Products And Raw materials |
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