229621-07-2

Basic information

• Product Name: trans-3,4-Bis(hydroxymethyl)-2,2,5,5-tetramethylpyrrolidin-1-yloxyl
• Synonyms: (3R,4R)-rel-3,4-Bis(hydroxymethyl)-2,2,5,5-tetramethyl-1-pyrrolidinyloxy
• CAS NO: 229621-07-2
• Molecular Formula: C10H20NO3
• Molecular Weight: 0
• Product Categories: Spin Labeling Compounds
• Mol File: 229621-07-2.mol
• Article Data: 1

Chemical Properties

• Melting Point: 189-191°C
• Boiling Point: 324.574°C at 760 mmHg
• Flash Point: 155.607°C
• Appearance: /
• Density: 1.066g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.485
• CAS DataBase Reference: trans-3,4-Bis(hydroxymethyl)-2,2,5,5-tetramethylpyrrolidin-1-yloxyl(CAS DataBase Reference)
• NIST Chemistry Reference: trans-3,4-Bis(hydroxymethyl)-2,2,5,5-tetramethylpyrrolidin-1-yloxyl(229621-07-2)
• EPA Substance Registry System: trans-3,4-Bis(hydroxymethyl)-2,2,5,5-tetramethylpyrrolidin-1-yloxyl(229621-07-2)

Safety Data

• Hazardous Substances Data: 229621-07-2(Hazardous Substances Data)

Usage

Chemical Properties

Yellow Solid

Uses

A spin label

InChI:InChI=1/C10H21NO3/c1-9(2)7(5-12)8(6-13)10(3,4)11(9)14/h7-8,12-14H,5-6H2,1-4H3/t7-,8-/m1/s1

Upstream product

• 119580-75-5 trans-3-methoxycarbonyl-2,2,5,5-tetramethyl-4-nitromethylpyrrolidin-1-oxyl 
• 229621-04-9 trans-4-Formyl-3-methoxycarbonyl-2,2,5,5-tetramethylpyrrolidin-1-yloxyl radical 

Downstream Products

• 229621-20-9 3,4-Bis(dibromomethyl)-2,5-dihydro-2,2,5,5-tetramethyl-1H-pyrrol-1-yloxyl radical 
• 229621-29-8 trans-3,4-Bis(iodomethyl)-2,2,5,5-tetramethylpyrrolidin-1-yloxyl radical 
• 229621-21-0 2,5-Dihydro-3,4-bis(methanesulfonylthiomethyl)-2,2,5,5-tetramethyl-1H-pyrrol-1-yloxyl radical 
• 229621-30-1 trans-3,4-Bis(methanesulfonylthiomethyl)-2,2,5,5-tetramethylpyrrolidin-1-yloxyl radical 

Relevant articles and documents

Synthesis and reactions of a symmetric paramagnetic pyrrolidine diene

Symmetric paramagnetic diene 6 was prepared and proved to be a useful intermediate in 1,4-addition, cheletropic, and Diels-Alder reactions. These methods were used for the synthesis of both aromatic 10, 12 heteroaromatic 15, 23 and heterocyclic ring fused