87587-01-7

Basic information

• Product Name: (E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide
• CAS NO: 87587-01-7
• Molecular Formula: C₁₀H₁₄N₄OS
• Molecular Weight: 238.3094
• Mol File: 87587-01-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 330°C at 760 mmHg
• Flash Point: 153.4°C
• Density: 1.19g/cm³
• Vapor Pressure: 1.26E-05mmHg at 25°C
• Refractive Index: 1.594
• CAS DataBase Reference: (E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide(87587-01-7)
• EPA Substance Registry System: (E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide(87587-01-7)

Safety Data

• Hazardous Substances Data: 87587-01-7(Hazardous Substances Data)

Usage

Description

(E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide, also known as N,N-dimethyl-2-[(1E)-1-(2-hydroxypyridin-1-yl)ethylidene]hydrazinecarbothioamide, is a chemical compound with the molecular formula C10H15N5OS. It is a thioamide derivative characterized by its potential applications in pharmaceutical and chemical research. This synthetic organic compound is involved in various chemical reactions and processes, necessitating careful handling and adherence to safety guidelines in laboratory settings.

Uses

Used in Pharmaceutical Research:
(E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide is used as a research compound for its potential applications in the development of new pharmaceuticals. Its unique chemical structure allows for exploration in drug discovery, particularly in the areas of medicinal chemistry and drug design.
Used in Chemical Research:
In the field of chemical research, (E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide serves as a valuable compound for studying its reactivity, stability, and potential use in the synthesis of other complex molecules. Its thioamide functionality may offer insights into new reaction pathways and mechanisms.
Used in Material Science:
(E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide may also find applications in material science, particularly in the development of novel materials with specific properties. Its unique structure could contribute to the creation of new materials with applications in various industries, such as electronics, energy, and environmental protection.
Used in Analytical Chemistry:
As an analytical chemistry tool, (E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide can be employed in the development of new analytical methods, such as chromatographic or spectroscopic techniques, for the detection and quantification of various compounds in complex samples.
Used in Chemical Education:
In the context of chemical education, (E)-2-[(1E)-1-(1-hydroxypyridin-2(1H)-ylidene)ethyl]-N,N-dimethyldiazenecarbothioamide can be utilized as a teaching aid to illustrate the principles of organic chemistry, reaction mechanisms, and the importance of molecular structure in determining a compound's properties and reactivity.

Upstream product

• 87587-00-6 methyl 3-<1-(2-pyridinyl 1-oxide)ethylidene>hydrazinecarbodithioate 
• 124-40-3 dimethyl amine 
• 2457-50-3 2-acetylpyridine N-oxide 
• 6926-58-5 4,4-dimethylthiosemicarbazide 
• 1122-62-9 2-acetylpyridine 

Relevant articles and documents

Complexes of Group 12 Metals with 2-Acetylpyridine 4N-Dimethylthiosemicarbazone and with 2-Acetylpyridine-N-oxide 4N-Dimethylthiosemicarbazone: Synthesis, Structure and Antifungal Activity

Reaction in ethanol of group 12 metal halides with 2-acetylpyridine 4N-dimethylthiosemicarbazone (H4DML) and with 2-acetylpyridine-N-oxide 4N-dimethylthiosemicarbazone (H4DMLO) afforded complexes of the forms [M(H4DML)X2] (1 - 9) and [M(H4DMLO)X2] (10 - 18) (M = ZnII, CdII or HgII; X = Cl, Br or I). H4DMLO and the complexes of both thiosemicarbazones have been characterized by elemental analysis and by IR and 1H, 13C and 113Cd NMR spectroscopy, and the crystal structures of [Cd(H4DML)Cl2] (4), [Cd(H4DML)I2] (6), H4DMLO, [Hg(H4DMLO)Cl2] (16) and [Hg(H4DMLO)Br2] (17) have been determined by X-ray diffractometry. In all the H4DML complexes, the thiosemicarbazone acts as an N,N,S-tridentate ligand, and the coordination polyhedra of the pentacoordinate metals are more or less distorted tetragonal pyramids. H4DMLO is an O,N,S-tridentate ligand for zinc and cadmium halides and an N,S-bidentate ligand for mercury halides, in which the mercury atom has coordination number four and a distorted trigonal pyramidal environment. In assays of antifungal activity against Aspergillus niger and Paecilomyces variotii, H4DML was more active than nystatin, and its complex with ZnCl2 also showed good activity against A. niger, neither H4DMLO nor any of its complexes inhibited the growth of either pathogen.