101325-43-3

Basic information

• Product Name: Benzenamine, 4,4'-(2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-diyl)bis[N,N-dimethyl-
• CAS NO: 101325-43-3
• Molecular Formula: C23H30N2O4
• Molecular Weight: 398.502
• Mol File: 101325-43-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4,4'-(2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-diyl)bis[N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4,4'-(2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-diyl)bis[N,N-dimethyl-(101325-43-3)
• EPA Substance Registry System: Benzenamine, 4,4'-(2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-diyl)bis[N,N-dimethyl-(101325-43-3)

Safety Data

• Hazardous Substances Data: 101325-43-3(Hazardous Substances Data)

Upstream product

• 100-10-7 4-dimethylamino-benzaldehyde 
• 82515-50-2 2,2-bis(hydroxymethyl)propane-1,3-diol 
• 115-77-5 Pentaerythritol 

Relevant articles and documents

Synthesis of diacetals by condensation of carbonyl compounds with bis(hydroxymethyl)-1,3-propanediol catalysed by expansive graphite

Synthesis of diacetals from 2,2-bis(hydroxymethyl)-1,3-propanediol with aldehydes and ketones under catalysis of expansive graphite in refluxing benzene or toluene in good to excellent yield has been described.

A green recyclable poly(4-vinylpyridine)-supported copper iodide nanoparticle catalyst for the chemoselective synthesis of pentaerythritol diacetals from aromatic aldehydes

Poly(4-vinylpyridine)-supported copper(I) iodide nanoparticles have been used as an efficient, green recyclable catalyst for the chemoselective synthesis of pentaerythritol diacetals from aromatic aldehydes and pentaerythritol under solvent-free conditions. This catalyst was reused six times without any loss of its activity.

A practical and efficient procedure for preparation of diacetals from 2,2-bis (hydroxymethyl) propane-1,3-diol with aldehydes and ketones catalysed by anhydrous ferrous sulfate

Synthesis of diacetals in excellent yields from aldehydes and ketones with 2,2-bis(hydroxymethyl)propane-1,3-diol is carried out in refluxing benzene or toluene with anhydrous ferrous sulfate as catalyst.