143782-25-6

Basic information

• Product Name: 2-(trifluoromethyl)-4-(3,4,4-trimethyl-5-oxo-2-thioxoimidazolidin-1-yl)benzonitrile
• Synonyms: 2-(Trifluoromethyl)-4-(3,4,4-trimethyl-5-oxo-2-thioxoimidazolidin-1-yl)benzonitrile; benzonitrile, 2-(trifluoromethyl)-4-(3,4,4-trimethyl-5-oxo-2-thioxo-1-imidazolidinyl)-
• CAS NO: 143782-25-6
• Molecular Formula: C₁₄H₁₂F₃N₃OS
• Molecular Weight: 327.3248
• Mol File: 143782-25-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 409°C at 760 mmHg
• Flash Point: 201.2°C
• Density: 1.44g/cm³
• Vapor Pressure: 6.69E-07mmHg at 25°C
• Refractive Index: 1.595
• CAS DataBase Reference: 2-(trifluoromethyl)-4-(3,4,4-trimethyl-5-oxo-2-thioxoimidazolidin-1-yl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(trifluoromethyl)-4-(3,4,4-trimethyl-5-oxo-2-thioxoimidazolidin-1-yl)benzonitrile(143782-25-6)
• EPA Substance Registry System: 2-(trifluoromethyl)-4-(3,4,4-trimethyl-5-oxo-2-thioxoimidazolidin-1-yl)benzonitrile(143782-25-6)

Safety Data

• Hazardous Substances Data: 143782-25-6(Hazardous Substances Data)

Usage

Physical form

White crystalline powder

Molecular weight

345.33 g/mol

Usage

Intermediate and raw material in the synthesis of pharmaceuticals and agrochemicals

Potential applications

Herbicide and fungicide

Role in research and development

Discovery of new drugs and therapeutics

Industrial and scientific applications

Versatile compound with various uses

Downstream Products

• 143782-31-4 4-(3,4,4-trimethyl-2,5-dioxo-1-imidazolidinyl)-2-trifluoromethyl-benzonitrile 

Relevant articles and documents

Phenylimidazolidines having antiandrogenic activity

A compound of the formula STR1 wherein R 1 is --CN, --NO 2 or halogen, R 2 is --CF 3 or halogen, --A-B-- is of STR2 X is --O-- or --S--, R 3 is hydrogen, alkyl, alkenyl or alkynyl of up to 12 carbon atoms, aryl and aralkyl of up to 12 carbon atoms, all optionally substituted by --OH, halogen, --SH, --CN, acyl and acyloxy of up to 7 carbon atoms, --aryl, --O--aryl, --O--aralkyl --S-- aryl of up to 12 carbon atoms the aryl and aralkyl being optionally substituted by halogen, --CF 3, alkyl, alkoxy, alkenyl, alkenyloxy, alkynyl or alkynyloxy with the sulfur being optionally oxidized to sulfone or sulfoxide, free, esterified, amidified or salified carboxy, --NH 2, mono and dialkylamino and heterocyclic of 3 to 6 ring members and containing at least one heteroatom selected from the group consisting of oxygen, sulfur and nitrogen, the alkyl, alkenyl and alkynyl being optionally interrupted by at least one oxygen, nitrogen or sulfur optionally oxidized to sulfoxide or sulfone, trialkylsilyl with the alkyl having 1 to 6 carbon atoms and acyl and acyloxy of an organic carboxylic acid of 1 to 7 carbon atoms and Y is --O--, --S-- or --NH--, except the compounds wherein --A-B-- is STR3 X is oxygen, R 3 is hydrogen and Y is oxygen or --NH--, R 2 is --CF 3 or halogen and R 1 is --NO 2 or halogen and their non-toxic, pharmaceutically acceptable acid addition salts.