CAS 61640-27-5

2H-Imidazole-2-thione, 1-(1,1-dimethylethyl)-1,3-dihydro-

Description:

2H-Imidazole-2-thione, 1-(1,1-dimethylethyl)-1,3-dihydro- is a heterocyclic organic compound characterized by its imidazole ring structure, which contains both nitrogen and sulfur atoms. This compound features a thione functional group, indicating the presence of a sulfur atom double-bonded to a carbon atom, contributing to its reactivity and potential biological activity. The presence of the tert-butyl group (1-(1,1-dimethylethyl)-) enhances its lipophilicity, which may influence its solubility and interaction with biological membranes. The compound is typically studied for its potential applications in pharmaceuticals, agrochemicals, and as a ligand in coordination chemistry. Its unique structure allows for various chemical modifications, making it a versatile building block in synthetic organic chemistry. Additionally, compounds of this nature may exhibit interesting properties such as antimicrobial or antifungal activities, although specific biological activities would require further investigation. Overall, 2H-Imidazole-2-thione derivatives are of significant interest in both academic and industrial research settings.

Formula: C₇H₁₂N₂S

1-(1,1-Dimethylethyl)-1,3-dihydro-2H-imidazole-2-thione

CAS: 61640-27-5

Formula: C₇H₁₂N₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 156.2486

Ref: IN-DA00372H

1-(tert-Butyl)-1,3-dihydro-2h-imidazole-2-thione

CAS: 61640-27-5

1-(tert-Butyl)-1,3-dihydro-2h-imidazole-2-thione

Purity: 98%

Ref: 54-OR1040654

1-tert-butyl-2,3-dihydro-1H-imidazole-2-thione

CAS: 61640-27-5

Purity: 98%

Molecular weight: 156.25

Ref: 10-F860712

1-tert-Butyl-1H-imidazole-2-thiol

CAS: 61640-27-5

1-tert-Butyl-1H-imidazole-2-thiol is a halogenated aromatic compound that is used as a solvent, a ligand in organometallic chemistry, and as an intermediate in the synthesis of other organic compounds. This chemical has been shown to undergo halide exchange reactions with metal ions such as magnesium chloride, aluminum chloride, and zinc chloride. It also has been shown to react with carboxylates to form 1-tert-butyl-1H-imidazole-2-carboxylate. The bond cleavage of the thiol group can be induced by reaction with iodosobenzene diacetate or hydrochloric acid. 1-tert-Butyl-1H-imidazole-2-thiol is soluble in ethers and benzene. The molecule has two thiol groups that can undergo disulfide bond formation, which may be catalyzed by copper(

Formula: C₇H₁₂N₂S

Purity: Min. 95%

Molecular weight: 156.25 g/mol

Ref: 3D-LCA64027