2305-59-1

Basic information

• Product Name: 4 4-DIMETHYL-2-IMIDAZOLINE 97
• Synonyms: 4 4-DIMETHYL-2-IMIDAZOLINE 97;5,5-Dimethyl-4,5-dihydro-1H-imidazole;4 4-DIMETHYL-2-IMIDAZOLINE 97%;4,4-dimethy-2-imidazoline;4,4-DIMETHY-2- IMIDAZOLINE 97%;4,5-Dihydro-4,4-dimethyl-1H-imidazole;5,5-dimethyl-1,4-dihydroimidazole
• CAS NO: 2305-59-1
• Molecular Formula: C₅H₁₀N₂
• Molecular Weight: 98.1463
• Mol File: 2305-59-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 80-85 °C/15 mmHg(lit.)
• Flash Point: 94 °C
• Appearance: /
• Density: 0.932 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.457mmHg at 25°C
• Refractive Index: n20/D 1.4701(lit.)
• Storage Temp.: -20°C
• PKA: 10.99±0.40(Predicted)
• CAS DataBase Reference: 4 4-DIMETHYL-2-IMIDAZOLINE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 4 4-DIMETHYL-2-IMIDAZOLINE 97(2305-59-1)
• EPA Substance Registry System: 4 4-DIMETHYL-2-IMIDAZOLINE 97(2305-59-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 2305-59-1(Hazardous Substances Data)

Usage

General Description

4 4-DIMETHYL-2-IMIDAZOLINE 97 is a chemical compound that is often used as a corrosion inhibitor in oil and gas production. It is a clear, colorless liquid with a slightly amine-like odor, and it is soluble in water. 4 4-DIMETHYL-2-IMIDAZOLINE 97 is known for its ability to effectively protect metal surfaces from corrosion, particularly in harsh environmental conditions. It is often used in the petroleum industry to prevent the degradation of equipment and infrastructure, and it is also utilized in the manufacturing of metalworking fluids and other industrial products. Additionally, 4 4-DIMETHYL-2-IMIDAZOLINE 97 has applications in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical compounds.

InChI:InChI=1/C5H10N2/c1-5(2)3-6-4-7-5/h4H,3H2,1-2H3,(H,6,7)

Upstream product

• 90304-06-6 (2-bromo-1,1-dimethylethyl)cyanamide 
• 1458-98-6 2-methyl-3-bromo-1-propene 
• 463-52-5 formamidine 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 
• 811-93-8 1,1-dimethylethylenediamine 
• 109-94-4 formic acid ethyl ester 
• 119072-55-8 tert-butylisonitrile 

Downstream Products

• 1146217-61-9 1,3-ditolyl-4,4-dimethyl-imidazolinium chloride 
• 291296-62-3 [Cu(4-amino-N-(thiazol-2-yl)benzenesulfonamide)2(4,4-dimethylimidazoline)2] 
• 73955-62-1 1-acetyl-2-(4-methoxy-phenyl)-3,4,4-trimethyl-imidazolidine 
• 73955-61-0 1-tosyl-3,4,4-trimethyl-2-imidazolidine 
• 89367-49-7 1-carbethoxy-2-<2'(4-methylbenzenesulphonyl)amine-1',1'-dimethyl>amino acrylic acid ethyl ester 
• 89367-45-3 1-acetyl-2-(4-chloro phenyl)-3,4,4-trimethylimidazolidine 
• 89367-44-2 1-acetyl-2-phenyl-3,4,4-trimethylimidazolidine 
• 71254-91-6 1-tosyl-3,4,4-trimethyl-Δ²-imidazolinium iodide 
• 71254-90-5 1-acetyl-3,4,4-trimethyl-Δ²-imidazolinium iodide 
• 141345-39-3 (5R^*,6R^*)-4-(benzyloxycarbonyl)-6-(benzyloxy)-2,2,6-trimethyl-1,4-diazabicyclo<3.2.0>heptan-7-one 
• 141345-41-7 (5R^*,6R^*)-4-(benzyloxycarbonyl)-2,2-dimethyl-1,4-diazabicyclo<3.2.0>heptan-7-one-6-spiro-2'-tetrahydrofuran 
• 141345-37-1 (5R^*,6R^*)-4-(benzyloxycarbonyl)-6-methoxy-2,2,6-trimethyl-1,4-diazabicyclo<3.2.0>heptan-7-one 
• 141345-45-1 (5S^*,6R^*)-6-(benzyloxy)-2,2,6-trimethyl-1,4-diazabicyclo<3.2.0>heptan-7-one 
• 141345-51-9 hexahydro-3,3,6-trimethyl-6-(phenylmethoxy)-5H-1,4-diazepin-5-one 

Relevant articles and documents

Effects of NHC-backbone substitution on efficiency in ruthenium-based olefin metathesis

A series of ruthenium olefin metathesis catalysts bearing N-heterocycliccarbene (NHC) ligands with varying degrees of backbone and N-aryl subst itution have been prepared. These complexes show greater resistance to decomposition through C-H activation of

Synthesis and complexation properties of poly(ethylene glycol)-linked mono- and bis-dioxocyclams

Both tri- and tetra(ethylene glycol) linked bis-chromium carbene complexes have been synthesized. These carbene complexes were photolyzed with N-protected imidazolines to give protected azapenams. These were transformed into polyether-linked basket dioxocyclams 4a,b and bis-dioxocyclams 5a,b. These compounds have cavities for the complexation of both 'hard' and 'soft' metal ions. The complexes of Ni, Ba, and Gd were synthesized.

A NEW REDUCTIVE PROCEDURE FOR THE PREPARATION OF VICINAL DIAMINES AND MONOAMINES

Selective reductive procedures for the preparation of vicinal diamines and monoamines from alkyl bromocyanamides are described.