CAS 1739-84-0

1,2-Dimethylimidazole

Description:

1,2-Dimethylimidazole is an organic compound characterized by its five-membered aromatic ring structure containing two nitrogen atoms. It is a derivative of imidazole, with two methyl groups attached to the first and second carbon atoms of the ring. This compound is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. It has a relatively low boiling point and is soluble in water and various organic solvents, making it versatile in chemical applications. 1,2-Dimethylimidazole exhibits basic properties due to the presence of nitrogen atoms, which can participate in protonation reactions. It is often used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other nitrogen-containing compounds. Additionally, it can act as a ligand in coordination chemistry and is utilized in various catalytic processes. Safety data indicates that it should be handled with care, as it may cause irritation upon contact with skin or eyes. Overall, 1,2-Dimethylimidazole is an important compound in both industrial and research settings.

Formula: C₅H₈N₂

InChI: InChI=1S/C5H8N2/c1-5-6-3-4-7(5)2/h3-4H,1-2H3

InChI key: InChIKey=GIWQSPITLQVMSG-UHFFFAOYSA-N

SMILES: CC=1N(C)C=CN1

Synonyms:

• 1,2-dimethyl-1H-imidazole
• 1,2Dmz
• 1H-Imidazole, 1,2-dimethyl-
• Curezol 1,2DMZ
• Dabco 2039
• Dabco 2040
• Dabco 2041
• Imidazole, 1,2-dimethyl-
• Kaolizer 390
• Lupragen DMI
• N,2-Dimethylimidazole
• NSC 111174
• Nichigo Imidazole 1,2-DMI
• Pc Cat Dmi
• SN 25 (vulcanizing agent)
• Sn 25
• Toyocat DM 70
• Toyocat DMI
• Toyocat DP 70

1,2-Dimethylimidazole

CAS: 1739-84-0

Formula: C₅H₈N₂

Purity: >98.0%(GC)

Color and Shape: White or Colorless to Light yellow powder to lump to clear liquid

Molecular weight: 96.13

Ref: 3B-D1562

1,2-Dimethylimidazole, 98%

CAS: 1739-84-0

1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts. This Thermo Scientific Chemicals bra

Formula: C₅H₈N₂

Purity: 98%

Color and Shape: Colorless to white to pale yellow, Crystals or powder or crystalline powder or fused solid or chunks

Molecular weight: 96.13

Ref: 02-B23544

1,2-Dimethyl-1H-imidazole

CAS: 1739-84-0

Formula: C₅H₈N₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 96.1304

Ref: IN-DA001Z9Y

1,2-Dimethylimidazole

CAS: 1739-84-0

Formula: C₅H₈N₂

Molecular weight: 96.13

Ref: 7W-GK8581

1,2-Dimethyl-1H-imidazole

CAS: 1739-84-0

1,2-Dimethyl-1H-imidazole is an imidazole derivative widely used in biochemical experiments and drug synthesis research.

Formula: C₅H₈N₂

Color and Shape: Solid

Molecular weight: 96.13

Ref: TM-TN9301

1,2-Dimethyl-1H-imidazole 98%

CAS: 1739-84-0

1,2-Dimethyl-1H-imidazole 98%

Purity: ≥95%

Molecular weight: 96.13042g/mol

Ref: 54-OR52033

1,2-Dimethyl-1H-imidazole

CAS: 1739-84-0

1,2-Dimethyl-1H-imidazole

Purity: 98%

Molecular weight: 96.13g/mol

Ref: 54-OR79826

1,2-Dimethylimidazole

CAS: 1739-84-0

Formula: C₅H₈N₂

Purity: 99.00%

Color and Shape: Low Melting Solid

Molecular weight: 96.133

Ref: 10-F093937

1,2-Dimethylimidazole

Controlled Product

CAS: 1739-84-0

Applications 1,2-DIMETHYLIMIDAZOLE (cas# 1739-84-0) is a useful research chemical.

Formula: C₅H₈N₂

Color and Shape: Light Yellow To Light Beige

Molecular weight: 96.13

Ref: TR-D460493

1,2-Dimethylimidazole

CAS: 1739-84-0

1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant.

Formula: C₅H₈N₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 96.13 g/mol

Ref: 3D-FD38774