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3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy, also known as 1-Oxyl-2,2,5,5,-tetramethyl-3-vinyl-△3-pyrroline, is a spin-labeled reagent derived from the pyrroline family of compounds. It is characterized by its unique structure, which includes a vinyl group and a tetramethylpyrrol ring, making it a versatile molecule for various applications in the field of biochemistry and molecular biology.

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  • 105843-07-0 Structure
  • Basic information

    1. Product Name: 3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy
    2. Synonyms: 1-Oxyl-2,2,5,5,-tetraMethyl-3-vinyl-3-pyrroline;3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy
    3. CAS NO:105843-07-0
    4. Molecular Formula: C10H16NO *
    5. Molecular Weight: 166.24014
    6. EINECS: N/A
    7. Product Categories: Heterocycles;Spin Labeling Compounds
    8. Mol File: 105843-07-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy(105843-07-0)
    11. EPA Substance Registry System: 3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy(105843-07-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 105843-07-0(Hazardous Substances Data)

105843-07-0 Usage

Uses

Used in Pharmaceutical Industry:
3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy is used as a spin-labeled reagent for the preparation of spin-labeled analogs of biologically active compounds. This application is particularly relevant in the pharmaceutical industry, where understanding the structure and function of biologically active molecules is crucial for drug discovery and development.
Used in the Preparation of Spin-Labeled Analogs:
3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy is used as a spin-labeled reagent for the preparation of spin-labeled analogs of various biologically active compounds, including Morphine, Nalorphine, Barbituric acid, Choline, and Acetylcholine. These spin-labeled analogs are essential tools in studying the structure, dynamics, and interactions of these molecules, which can provide valuable insights into their biological functions and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 105843-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,4 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105843-07:
(8*1)+(7*0)+(6*5)+(5*8)+(4*4)+(3*3)+(2*0)+(1*7)=110
110 % 10 = 0
So 105843-07-0 is a valid CAS Registry Number.

105843-07-0SDS

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 1-oxyl-3-vinyl-2,2,5,5-tetramethyl-3-pyrroline

1.2 Other means of identification

Product number -
Other names 1-Oxyl-2,2,5,5,-tetramethyl-3-vinyl-3-pyrroline

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:105843-07-0 SDS

105843-07-0Downstream Products

105843-07-0Relevant articles and documents

Further syntheses with nitroxide &α,&β-unsaturated aldehydes and allylic bromides

Hideg, Kalman,Csekeo, Jozsef,Hankovszky, H. Olga,Sohar, Pal

, p. 1482 - 1490 (2007/10/02)

The enhanced reactivity of nitroxide allylic bromides is used for preparation of spin-labelled analogues of biologically active compounds (morphine, Nalorphine, barbituric acid, choline and acetyl choline).Nitroxide α,β-unsaturated aldehydes are reacted with phosphoranes to give nitroxide polyenes.The nitroxides are reduced to diamagnetic N-hydroxy hydrochloride salts, which can be converted in the presence of base to N-acetoxy derivatives.

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