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1-methyl-2,3,4,5,6,7-hexahydro-1H-phosphindole 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57065-64-2

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57065-64-2 Usage

Type

Synthetic organophosphorus compound

Properties

+ Stable nitroxide
+ Used as a spin label in electron paramagnetic resonance spectroscopy
+ Potential application as a contrast agent in magnetic resonance imaging
+ Studied as a radical probe in biological systems
+ Valuable tool for studying kinetics and dynamics of radical processes
+ Exhibits antioxidant properties
+ Investigated for potential therapeutic applications in treatment of oxidative stress-related diseases

Structure

Hexahydro-1H-phosphindole with a 1-oxide group and a methyl group at the 1-position.

Check Digit Verification of cas no

The CAS Registry Mumber 57065-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,6 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57065-64:
(7*5)+(6*7)+(5*0)+(4*6)+(3*5)+(2*6)+(1*4)=132
132 % 10 = 2
So 57065-64-2 is a valid CAS Registry Number.

57065-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-2,3,4,5,6,7-hexahydrophosphindole 1-oxide

1.2 Other means of identification

Product number -
Other names 1-methyl-2,3,4,5,6,7-hexahydro-phosphindole 1-oxide

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:57065-64-2 SDS

57065-64-2Relevant academic research and scientific papers

Inter- and Intramolecular Arylation of the Double Bond in Phospholene Derivatives under Friedel-Crafts Conditions

MacDiarmid, Joan E.,Quin, Louis D.

, p. 1451 - 1456 (2007/10/02)

Reaction between benzene or chlorobenzene with the double bond of certain phospholene derivatives occurs in the presence of aluminum chloride at room temperature to yield β-arylated phospholanes.Phospholene derivatives employed in such reactions have incl

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