868961-34-6

Basic information

• Product Name: oxo-(2,4,6-trimethylphenylamino)acetyl chloride
• Synonyms: oxo-(2,4,6-trimethylphenylamino)acetyl chloride
• CAS NO: 868961-34-6
• Molecular Weight: 225.675
• Mol File: 868961-34-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: oxo-(2,4,6-trimethylphenylamino)acetyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: oxo-(2,4,6-trimethylphenylamino)acetyl chloride(868961-34-6)
• EPA Substance Registry System: oxo-(2,4,6-trimethylphenylamino)acetyl chloride(868961-34-6)

Safety Data

• Hazardous Substances Data: 868961-34-6(Hazardous Substances Data)

Upstream product

• 79-37-8 oxalyl dichloride 
• 88-05-1 2,4,6-trimethylaniline 
• 79354-46-4 2-(2,4,6-trimethylphenylamino)-2-oxoacetic acid 
• 79354-30-6 2-(2,4,6-trimethylphenylamino)-2-oxoacetic acid ethyl ester 

Downstream Products

• 868961-35-7 N-(4-bromo-2,6-dimethylphenyl)-N'-(2,4,6-trimethylphenyl)oxamide 
• 951695-89-9 N-(2-(isopropylthio)phenyl)-N'-(mesityl)-oxalamide 
• 941984-17-4 N-cyclohexyl-N'-(2,4,6-trimethylphenyl)oxalamide 
• 1071505-61-7 C₂₈H₃₀N₄O₄ 
• 1071505-64-0 C₃₈H₄₂N₄O₄ 
• 1071505-63-9 C₃₆H₃₈N₄O₄ 

Relevant articles and documents

Lipase active site covalent anchoring of Rh(NHC) catalysts: Towards chemoselective artificial metalloenzymes

A Rh(NHC) phosphonate complex reacts with the lipases cutinase and Candida antarctica lipase B resulting in the first (soluble) artificial metalloenzymes formed by covalent active site-directed hybridization. When compared to unsupported complexes, these

Palladium-catalyzed arylation of aldehydes with bromo-substituted 1,3-diaryl-imidazoline carbene ligand

The combination of 0 valent palladium precursor and bromo-substituted 1,3-diaryl-imidazoline carbene ligand precursor such as 1-(2-bromophenyl)-3-(2,6-diisopropylphenyl)-imidazolinium chloride 1a exhibited high catalytic activity for the 1,2-addition of arylboronic acids to aldehydes including aqueous formaldehyde.

Homodinuclear ruthenium catalysts for dimer ring-closing metathesis

(Chemical Equation Presented) Two ring or not to ring: Novel diruthenium olefin metathesis catalysts show a tendency to avoid oligomerization and favor cyclic dimerization when the distances between the ruthenium centers and between the diene extremities match (see scheme).