79354-30-6

Basic information

• Product Name: Acetic acid, oxo[(2,4,6-trimethylphenyl)amino]-, ethyl ester
• CAS NO: 79354-30-6
• Molecular Formula: C13H17NO3
• Molecular Weight: 235.283
• Mol File: 79354-30-6.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Acetic acid, oxo[(2,4,6-trimethylphenyl)amino]-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, oxo[(2,4,6-trimethylphenyl)amino]-, ethyl ester(79354-30-6)
• EPA Substance Registry System: Acetic acid, oxo[(2,4,6-trimethylphenyl)amino]-, ethyl ester(79354-30-6)

Safety Data

• Hazardous Substances Data: 79354-30-6(Hazardous Substances Data)

Upstream product

• 4755-77-5 Ethyl oxalyl chloride 
• 88-05-1 2,4,6-trimethylaniline 

Downstream Products

• 1510834-01-1 N¹-(2,4,6-trimethylphenyl)-N²-(2-hydroxybenzyl)-1,2-diaminoethane 

Relevant articles and documents

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Bis-ligated titanium (IV) metal complexes supported by bidentate unsymmetrical o-hydroxyaryl-substituted N-heterocyclic carbene ligands were synthesized and structurally identified. While the direct addition of the doubly deprotonated bulky imidazolidiniu

Chiral secondary phosphine oxide pre-ligand and application thereof

The invention discloses a chiral secondary phosphine oxide pre-ligand and application thereof. The structure of the ligand is as shown in Formula I, where R. 1 . R2 , R3 And R4 Hydrogen, benzyl, substituted alkyl, substituted or unsubstituted aryl. The more preferred structural formula comprises 4 structural general formulas shown in the general formula I in the following formula: I-d, and the formula is shown in the general formula. Based on the designed asymmetric catalytic reaction system, the stability and the easy preparation of the comprehensive test ligand under the hydrocarbon activation condition are synthesized, and finally the chiral secondary oxidation phosphorus precursor with the double functional groups in the oxidation and heating environment is selected. The catalyst formed by the front ligand and the active metal compound has high activity and high selectivity in the reaction of constructing a chiral center, and has the stability.

Visible-light mediated carbamoyl radical addition to heteroarenes

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