H-HOMOPRO-OME HCL

H-HOMOPRO-OME HCL Structure
CAS No.
18650-39-0
Chemical Name:
H-HOMOPRO-OME HCL
Synonyms
L-PIP-OME;H-HOPRO-OME HCL;H-PIC(2)-OME HCL;L-HOMOPRO-OME-HCL;H-HOMOPRO-OME HCL;HOMOPROLINE-OME HCL;L-PIPECOLIC ACID-OME HCL;Homoproline-OMe Hydrochloride;L-HOMO-PROLINE METHYL ESTER HCL;METHYL L-PIPECOLATE HYDROCHLORIDE
CBNumber:
CB4711960
Molecular Formula:
C7H14ClNO2
Molecular Weight:
179.64
MOL File:
18650-39-0.mol
Modify Date:
2023/4/23 13:52:06

H-HOMOPRO-OME HCL Properties

Melting point 176-177℃
storage temp. Inert atmosphere,2-8°C
form powder
color White to off-white

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332-H315-H319
Precautionary statements  P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P302+P352+P312-P304+P340+P312
HS Code  2933399990

H-HOMOPRO-OME HCL Chemical Properties,Uses,Production

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.

H-HOMOPRO-OME HCL Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 121)Suppliers
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(S)-PIPERIDINE-2-CARBOXYLIC ACID METHYL ESTER HCL (S)-PIPERIDINE-2-CARBOXYLIC ACID METHYL ESTER HYDROCHLORIDE L-HOMO-PROLINE METHYL ESTER HCL L-HOMOPROLINE METHYL ESTER HYDROCHLORIDE L-HOMOPRO-OME-HCL L-2-PIPECOLIC ACID METHYL ESTER HCL L-2-PIPECOLIC ACID METHYL ESTER HYDROCHLORIDE H-HOPRO-OME HCL H-HOMOPRO-OME HCL H-PIC(2)-OME HCL HOMOPROLINE-OME HCL METHYL (S)-PIPERIDINECARBOXYLATE HYDROCHLORIDE METHYL L-PIPECOLATE HYDROCHLORIDE L-PIP-OME L-PIPECOLINIC ACID METHYL ESTER HYDROCHLORIDE L-PIPECOLIC ACID METHYL ESTER HYDROCHLORIDE L-PIPECOLIC ACID-OME HCL Homoproline-OMe Hydrochloride L-Pipecolic Acid-OMe Hydrochloride (L)-(-)-(S)-Piperidine-2-carboxylic acid Methyl ester HCl salt Methyl (2S)-piperidine-2-carboxylate hydrochloride 2-Piperidinecarboxylic acid, Methyl ester, hydrochloride, (2S)- (L)-(-)-(S)-Piperidine-2-carboxylic acid Methyl ester 2-Piperidinecarboxylic acid, Methyl ester, hydrochloride (1:1), (2S)- R-2-Piperidinecarboxylic acid 1,1-diMethylethyl ester (S)-Methyl piperidine-2-carboxylate HCl Methyl(2S)-piperidinecarboxylatehydrochloride (S)-methyl piperidine-2-carboxylate (S)-Methyl piperidine-2-carboxylate hydrochloride Methyl (S)-piperidine-2-carboxylate hydrochloride (L)-(-)-(S)-Piperidine-2-carboxylic acid methyl ester HCl (S)-methyl pipecolinate hydrochloride methyl(2S)-piperidine-2-carboxylate (2S)-2-Piperidinecarboxylic acid methyl ester hydrochloride (1:1) 18650-39-0 pharmacetical