Identification | Back Directory | [Name]
H-HOMOPRO-OME HCL | [CAS]
18650-39-0 | [Synonyms]
L-PIP-OME H-HOPRO-OME HCL H-PIC(2)-OME HCL H-HOMOPRO-OME HCL L-HOMOPRO-OME-HCL HOMOPROLINE-OME HCL L-PIPECOLIC ACID-OME HCL Homoproline-OMe Hydrochloride L-HOMO-PROLINE METHYL ESTER HCL METHYL L-PIPECOLATE HYDROCHLORIDE L-2-PIPECOLIC ACID METHYL ESTER HCL (S)-methyl piperidine-2-carboxylate methyl(2S)-piperidine-2-carboxylate L-Pipecolic Acid-OMe Hydrochloride (S)-methyl pipecolinate hydrochloride (S)-Methyl piperidine-2-carboxylate HCl L-HOMOPROLINE METHYL ESTER HYDROCHLORIDE L-PIPECOLIC ACID METHYL ESTER HYDROCHLORIDE L-PIPECOLINIC ACID METHYL ESTER HYDROCHLORIDE L-2-PIPECOLIC ACID METHYL ESTER HYDROCHLORIDE Methyl(2S)-piperidinecarboxylatehydrochloride METHYL (S)-PIPERIDINECARBOXYLATE HYDROCHLORIDE (S)-PIPERIDINE-2-CARBOXYLIC ACID METHYL ESTER HCL (S)-Methyl piperidine-2-carboxylate hydrochloride Methyl (S)-piperidine-2-carboxylate hydrochloride Methyl (2S)-piperidine-2-carboxylate hydrochloride R-2-Piperidinecarboxylic acid 1,1-diMethylethyl ester (L)-(-)-(S)-Piperidine-2-carboxylic acid Methyl ester (L)-(-)-(S)-Piperidine-2-carboxylic acid methyl ester HCl (S)-PIPERIDINE-2-CARBOXYLIC ACID METHYL ESTER HYDROCHLORIDE (L)-(-)-(S)-Piperidine-2-carboxylic acid Methyl ester HCl salt 2-Piperidinecarboxylic acid, Methyl ester, hydrochloride, (2S)- 2-Piperidinecarboxylic acid, Methyl ester, hydrochloride (1:1), (2S)- | [Molecular Formula]
C7H14ClNO2 | [MDL Number]
MFCD00672366 | [MOL File]
18650-39-0.mol | [Molecular Weight]
179.64 |
Hazard Information | Back Directory | [Uses]
Methyl (2S)-Piperidine-2-carboxylate Hydrochloride can be useful in the preparation of Thyrotropin-?releasing hormone (TRH) analogs, preparation of (arylsulfonyl)(amidino)phenylalanine piperidinamides as matriptase inhibitors, stereoselective synthesis of protected peptides containing anti β-hydroxy tyrosine, preparation of analogs of endogenous neuropeptide cycloprolylglycine, and preparation of promysalin analogs. It can also be useful in the preparation of molecular switches within ADX-47273 mGlu5 PAM scaffold that modulate modes of pharmacology to afford mGlu5 modulators. |
|
|