L-Glu.OBZl

L-Glu.OBZl - Names and Identifiers

Name	(S)-3-Piperidinecarboxylic acid methyl ester hydrochloride
Synonyms	L-Glu.OBZl (S)-Methyl piperidine-3-carboxylate HCl (S)-3-Piperidinecarboxylic acid methyl ester HCl METHYL (S)-PIPERIDINE-3-CARBOXYLATE HYDROCHLORIDE (S)-3-METHYL PIPERIDINE CARBOXYLATE HYDROCHLORIDE (S)-Methyl piperidine-3-carboxylate hydrochloride (S)-3-Methyl Piperidine Carboxylate Hydrochloride methyl (3S)-piperidine-3-carboxylate hydrochloride (S)-3-Piperidinecarboxylic acid methyl ester hydrochloride
CAS	164323-84-6
InChI	InChI=1/C7H13NO2.ClH/c1-10-7(9)6-3-2-4-8-5-6;/h6,8H,2-5H2,1H3;1H/t6-;/m0./s1

L-Glu.OBZl - Physico-chemical Properties

Molecular Formula	C7H14ClNO2
Molar Mass	179.64
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C
Use	This product is for scientific research only and shall not be used for other purposes.

L-Glu.OBZl - Risk and Safety

Risk Codes	36 - Irritating to the eyes
Safety Description	26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

L-Glu.OBZl - Introduction

(S)-3-Piperidinecarboxylic acid methyl ester hydrochloride is an organic compound with the molecular formula C12H18ClNO2. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance:(S)-3-Piperidinecarboxylic acid methyl ester hydrochloride is usually colorless to light yellow crystalline or solid.
-Solubility: It is slightly soluble in water, but it is more soluble in some organic solvents such as ethanol and dimethyl sulfoxide.
-Melting point: Its melting point range is 80-85°C.
-Optical activity: The compound is an optical isomer with optical rotation, and its optical rotation is

S:[α]25D = -29±1 ° (c = 1, CHCl3)

R:[α]25D = 29±1 ° (c = 1, CHCl3)

Use:
(S)-3-Piperidinecarboxylic acid methyl ester hydrochloride has a wide range of applications in organic synthesis:
-It can be used as a catalyst and reagent for asymmetric addition reactions in enantioselective synthesis.
-It is also commonly used in the synthesis of drugs, pesticides, spices and other organic compounds.
-It can also be used for other asymmetric catalytic reactions in organic synthesis.

Method:
Generally,(S)-3-Piperidinecarboxylic acid methyl ester hydrochloride is obtained by esterification of (S)-3-Piperidinecarboxylic acid. The esterification reaction usually uses methanol and thionyl chloride as reactants and is carried out at an appropriate temperature.

Safety Information:
- (S)-3-Piperidinecarboxylic acid methyl ester hydrochloride should be kept away from high temperatures, open flames and oxidants.
-Wear appropriate personal protective equipment, such as goggles and gloves.
-Avoid contact with skin, eyes and respiratory tract. If contact causes irritation, rinse with plenty of water and seek medical treatment.
-In the use and storage, should strictly adhere to the chemical safety procedures.

Last Update：2024-04-09 02:00:42