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1-CBZ-3-(2-Hydroxy-ethyl)-piperidine is a pharmaceutical intermediate and a piperidine derivative. It features a central piperidine ring, which is a common structural element in many pharmaceuticals and biologically active compounds. The presence of the 2-hydroxy-ethyl group suggests potential hydrophilic properties, improving its solubility in water. The CBZ (carbobenzyloxy) group serves as a protective moiety. However, specific uses, chemical properties, toxicity, and safety profiles are not extensively documented in public chemistry databases and may require further research.

115909-93-8

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115909-93-8 Usage

Uses

Used in Pharmaceutical Industry:
1-CBZ-3-(2-HYDROXY-ETHYL)-PIPERIDINE is used as a building block for the synthesis of more complex chemical compounds, particularly in the development of new pharmaceuticals. Its hydrophilic characteristics and protective carbobenzyloxy group make it a valuable intermediate in the creation of drugs with improved solubility and bioavailability.

Check Digit Verification of cas no

The CAS Registry Mumber 115909-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,9,0 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115909-93:
(8*1)+(7*1)+(6*5)+(5*9)+(4*0)+(3*9)+(2*9)+(1*3)=138
138 % 10 = 8
So 115909-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H21NO3/c17-10-8-13-7-4-9-16(11-13)15(18)19-12-14-5-2-1-3-6-14/h1-3,5-6,13,17H,4,7-12H2/t13-/m1/s1

115909-93-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-CBZ-3-(2-HYDROXY-ETHYL)-PIPERIDINE

1.2 Other means of identification

Product number -
Other names 3-(2-HYDROXY-ETHYL)-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:115909-93-8 SDS

115909-93-8Relevant articles and documents

Copper-catalyzed enantioselective intramolecular alkylboron allylic alkylation

Hojoh, Kentaro,Shido, Yoshinori,Ohmiya, Hirohisa,Sawamura, Masaya

supporting information, p. 632 - 635 (2018/04/23)

A reductive CC-bond-forming cyclization of vinyl-terminated allyl chlorides via alkene hydroboration with 9-BBN-H followed by Cu-catalyzed asymmetric intramolecular allylic alkylation with a new chiral phosphoramidite ligand produced six-membered ring com

Synthese und Bestimmung des Chiralitaetssinns von (+)-(R)-1-Azabicyclononan-2-on

Brehm, Renate,Ohnhaeuser, Dieter,Gerlach, Hans

, p. 1981 - 1987 (2007/10/02)

Optically active (+)-(R)-1-azabicyclononan-2-one ((+)-1) of known absolute configuration is synthesized in the following way: Resolution of (+/-)-piperidin-3-ethanol ((+/-)-2) by fractional recrystallization of its diastereoisomeric salts with (+)-

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