S-1-CBZ-3-Hydroxy-piperidine

S-1-CBZ-3-Hydroxy-piperidine Suppliers list
Company Name: Chembest Research Laboratories Limited  
Tel: 021-20908456
Email: sales@BioChemBest.com
Company Name: Shanghai Jian Chao Chemical Technology Co., Ltd.  
Tel: 150-2103-5486 18017383231
Email: 983544897@qq.com
Company Name: Acesys Pharmatech  
Tel: 18860950986
Email: tangmanman@zenjipharma.com
Company Name: Chengdu Firster Pharmaceutical Co., Ltd.  
Tel: 028-87078428 028-87074958
Email: chengzhenyong@cdfirster.com
Company Name: Cool Pharm, Ltd  
Tel: 021-60455363 18019463053
Email: sales@coolpharm.com

S-1-CBZ-3-Hydroxy-piperidine manufacturers

S-1-CBZ-3-Hydroxy-piperidine Basic information
Product Name:S-1-CBZ-3-Hydroxy-piperidine
Synonyms:benzyl (3S)-3-hydroxypiperidine-1-carboxylate;S-1-CBZ-3-Hydroxy-piperidine;(S)-1-Cbz-3-hydroxy-piper...;(S)-Benzyl 3-hydroxypiperidine-1-carboxylate;(3S)-3-Hydroxy-1-piperidinecarboxylic acid phenylmethyl ester;Benzyl (3S)-3-hydroxy-1-piperidinecarboxylate;1-Piperidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester, (3S)-
CAS:94944-69-1
MF:C13H17NO3
MW:235.28
EINECS:
Product Categories:
Mol File:94944-69-1.mol
S-1-CBZ-3-Hydroxy-piperidine Structure
S-1-CBZ-3-Hydroxy-piperidine Chemical Properties
Boiling point 384.9±42.0 °C(Predicted)
density 1.220±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka14.72±0.20(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
S-1-CBZ-3-Hydroxy-piperidine Usage And Synthesis
Synthesis
1-N-CBZ-3-PIPERIDONE

61995-20-8

S-1-CBZ-3-Hydroxy-piperidine

94944-69-1

General procedure for the synthesis of benzyl (S)-3-hydroxypiperidine-1-carboxylate from 1-N-Cbz-3-piperidone: a reaction mixture of 1 mL of potassium phosphate buffer (100 mM, pH 7.0) containing 200 mM substrate (1-N-Cbz-3-piperidone), 1 mM NAD+, 5% (v/v) 2-propanol, and 10 mg of crude enzyme READH was incubated at 50°C warming. For ChKRED20, the reaction conditions were adjusted to contain 40% (v/v) 2-propanol and the reaction temperature was 40°C. The reaction progress was monitored by TLC and the reaction was extracted with methyl tert-butyl ether (1 mL) at the termination of the reaction. The organic phase was dried with anhydrous sodium sulfate and concentrated. The conversion and enantiomeric excess were determined by chiral HPLC. The products were purified by silica gel column chromatography and structurally characterized by NMR analysis, spinometry and mass spectrometry.

References[1] Process Biochemistry, 2017, vol. 56, p. 90 - 97
S-1-CBZ-3-Hydroxy-piperidine Preparation Products And Raw materials
Raw materials1-N-Cbz-3-piperidone-->BETA-DPN LITHIUM SALT-->Isopropyl alcohol
Tag:S-1-CBZ-3-Hydroxy-piperidine(94944-69-1) Related Product Information
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