73604-52-1

Basic information

• Product Name: 2,4,4-TRIMETHYL-PYRROLIDINE
• Synonyms: 2,4,4-TRIMETHYL-PYRROLIDINE
• CAS NO: 73604-52-1
• Molecular Formula: C₇H₁₅N
• Molecular Weight: 113.2007
• Mol File: 73604-52-1.mol
• Article Data: 73

Chemical Properties

• Boiling Point: 121.6±8.0 °C(Predicted)
• Appearance: /
• Density: 0.790±0.06 g/cm3(Predicted)
• PKA: 11.00±0.10(Predicted)
• CAS DataBase Reference: 2,4,4-TRIMETHYL-PYRROLIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,4-TRIMETHYL-PYRROLIDINE(73604-52-1)
• EPA Substance Registry System: 2,4,4-TRIMETHYL-PYRROLIDINE(73604-52-1)

Safety Data

• Hazardous Substances Data: 73604-52-1(Hazardous Substances Data)

Usage

General Description

2,4,4-Trimethyl-pyrrolidine is a chemical compound with the molecular formula C8H17N. It is a colorless liquid with a strong amine-like odor and is primarily used as a solvent in the manufacturing of various products such as pharmaceuticals, pesticides, and polymers. It is also used as a corrosion inhibitor and in the production of dyes and pigments. 2,4,4-Trimethyl-pyrrolidine is considered to be a low acute toxicity substance, with no significant health hazards associated with its use at normal levels. However, it may cause irritation to the skin, eyes, and respiratory tract upon direct contact or inhalation. It is important to handle and use this chemical with appropriate safety measures in place to avoid any potential risks.

Upstream product

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• 7647-01-0 hydrogenchloride 
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Relevant articles and documents

Investigating a Redox Active Samarium Complex in Catalytic Reactions

Herein the synthesis of a new ethynyl ferrocenyl amidinate ligand [Fc?C≡C-{C(Ndipp)2H}] (Fc=ferrocenyl; dipp=diisopropylphenyl) and the subsequent formation of the corresponding samarium amido complex [Sm{Fc?C≡C-[C(Ndipp)2]}2/s

Bora-amidinate as a cooperative ligand in group 2 metal catalysis

Syntheses and crystal structures of the monomeric bora-amidinate (bam) complexes DIPPNBN-Mg·(THF)3 and DIPPNBN-Ca·(THF)4 are presented; DIPPNBN = HB[N(2,6-iPr2-C6H3)]

Cyclopentadienyl-based Mg complexes in the intramolecular hydroamination of aminoalkenes: Mechanistic evidence for cationic: Versus neutral magnesium derivatives

Neutral and cationic magnesium complexes stabilized by coordination of a cyclopentadienyl ligand with two different neutral hemilabile donor groups [Mg{η5-C5H3-1,3-(CH2CH2NiPr2)(SiMe2NPh2)}X(thf)] (X = Bz (2); N(SiMe3)2 (3)) and [Mg{η5-C5H3-1,3-(CH2CH2NiPr2)(SiMe2NPh2)}][BPh4] (4) have been prepared and characterized. The 1H-13C HMBC and HSQC spectra of compounds 2 and 3 demonstrate the formation of 1,3-substituted cyclopentadienyl compounds and DOSY and 1H-NMR experiments support the coordination-decoordination in solution of a THF molecule in complex 2. No Schlenk-type ligand redistributions were observed in the chemical behaviour of these magnesium complexes. Compounds 2-4 are active catalysts in the hydroamination of aminoalkenes; stoichiometric reactions and kinetic measurements have been performed to gain an insight into their reaction mechanisms. A key contribution here is the catalytic reactivity of a cationic magnesium compound.