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1-Pyrrolidinyloxy, 2,5-dimethyl-2,5-diphenyl-, (2S,5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

182212-33-5

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182212-33-5 Usage

Type of compound

Stable nitroxide radical

Use

Spin label in electron paramagnetic resonance (EPR) spectroscopy

Chirality

Chiral compound with two stereocenters

Most common isomer

(2S,5S)-isomer

Known for

High stability and strong spin-spin interaction

Applications

Studying molecular dynamics and interactions in biological systems, contrast agent in magnetic resonance imaging (MRI), and radical scavenger for studying oxidative stress in biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 182212-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,2,1 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 182212-33:
(8*1)+(7*8)+(6*2)+(5*2)+(4*1)+(3*2)+(2*3)+(1*3)=105
105 % 10 = 5
So 182212-33-5 is a valid CAS Registry Number.

182212-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-(2S,5S)-2,5-dimethyl-2,5-diphenylpyrrolidine-1-oxyl

1.2 Other means of identification

Product number -
Other names (2S,5S)-2,5-dimethyl-2,5-diphenylpyrrolidin-1-oxy radical

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:182212-33-5 SDS

182212-33-5Downstream Products

182212-33-5Relevant academic research and scientific papers

Synthesis, resolution and crystal structure of a new optically active nitroxide radical

Benfaremo, Nicholas,Steenbock, Marco,Klapper, Markus,Muellen, Klaus,Enkelmann, Volker,Cabrera, Karin

, p. 1413 - 1415 (2007/10/03)

The synthesis of the readily available racemate of the nitroxide radical 5 is described. The product exhibits exclusively the irons configuration. The cis product was not obtained. Optically pure enantiomers of 5 were isolated in gram quantities by chiral HPLC. Thus, separation of the enantiomers of a nitroxide radical was achieved for the first time. The structure of 5 was proven by a single-crystal diffraction study. VCH Verlagsgesellschaft mbH, 1996.

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