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660862-46-4

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660862-46-4 Usage

General Description

2-Piperazineethanol, (2R)-(9CI) is a chemical compound with the molecular formula C6H14N2O. It is a chiral compound, meaning it has a specific spatial arrangement of atoms. This chemical is commonly used as a reactant in the synthesis of pharmaceutical compounds, particularly in the production of antihistamines and antipsychotic drugs. It is also used as a building block in the preparation of various organic compounds. Additionally, 2-Piperazineethanol, (2R)-(9CI) has potential applications in the field of medicinal chemistry and drug discovery due to its pharmacological properties. Its unique structure and reactivity make it a valuable tool for the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 660862-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,0,8,6 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 660862-46:
(8*6)+(7*6)+(6*0)+(5*8)+(4*6)+(3*2)+(2*4)+(1*6)=174
174 % 10 = 4
So 660862-46-4 is a valid CAS Registry Number.

660862-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-piperazin-2-yl-ethanol

1.2 Other means of identification

Product number -
Other names (R)-2-piperazin-2-ylethanol

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:660862-46-4 SDS

660862-46-4Relevant articles and documents

A Versatile Synthesis of Vinyl-Substituted Heterocycles via Regio- And Enantioselective Pd-Catalyzed Tandem Allylic Substitution

Qian, Chao,Tang, Wenjun,Tang, Wenjun

supporting information, p. 4483 - 4488 (2020/06/05)

We herein report a versatile, regio- and enantioselective palladium-catalyzed tandem allylic substitution powered by a chiral bisphosphorus ligand WingPhos with the palladium loading as low as 0.1 mol %, forming a series of chiral vinyl-substituted heterocycles, including tetrahydroquinoxalines, piperazines, dihydro-2H-benzo[b][1,4]-oxazines, and morpholines, in exellent ee's and yields. The protocol features readily available starting materials, mild reaction conditions, and a broad substrate scope. Mechanistic investigation supports a tandem allylic substitution process.

NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS

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Page/Page column 15, (2010/02/12)

Acetylcholine receptor ligands of formula (I), wherein D, Ar1, E and Ar2 are as described in the specification, diastereoisomers, enantiomers, pharmaceutically-acceptable salts, methods of making, pharmaceutical compositions containing and methods for usi

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