34824-32-3

Basic information

• Product Name: Benzoyl chloride, 2,4,5-trimethyl- (7CI,9CI)
• Synonyms: Benzoyl chloride, 2,4,5-trimethyl- (7CI,9CI)
• CAS NO: 34824-32-3
• Molecular Formula: C₁₀H₁₁ClO
• Molecular Weight: 182.64674
• Product Categories: ACIDHALIDE
• Mol File: 34824-32-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 274.1±9.0 °C(Predicted)
• Appearance: /
• Density: 1.109±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzoyl chloride, 2,4,5-trimethyl- (7CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 2,4,5-trimethyl- (7CI,9CI)(34824-32-3)
• EPA Substance Registry System: Benzoyl chloride, 2,4,5-trimethyl- (7CI,9CI)(34824-32-3)

Safety Data

• Hazardous Substances Data: 34824-32-3(Hazardous Substances Data)

Upstream product

• 528-90-5 2,4,5-trimethylbenzoic acid 

Downstream Products

• 102948-88-9 pyren-1-yl-(2,4,5-trimethyl-phenyl)-ketone 
• 92492-87-0 2,4,5-trimethyl-benzoic acid-(2-dimethylamino-ethylamide) 
• 34824-33-4 9-(2,4,5-Trimethyl-benzoyl)-phenanthren 
• 145192-95-6 N-cycloheptyl-2,4,6-trimethylbenzamide 
• 114056-73-4 2,4,5-trimethylbenzohydroxamic acid 
• 123103-15-1 9-(2,4,5-Trimethyl-benzoyl)-1,2,3,4-tetrahydro-phenanthren 
• 69186-97-6 2,4,5-Trimethyl-benzoic acid 2,2-dimethyl-1-(2,4,5-trimethyl-phenyl)-propyl ester 
• 937261-48-8 2,4,5,N-tetramethyl-benzamide 
• 145192-96-7 N-<(1S)-4-oxocycloheptyl>-2,4,6-trimethylbenzamide 
• 114056-83-6 (3-Hydroxy-isoxazolidin-2-yl)-(2,4,5-trimethyl-phenyl)-methanone 

Relevant articles and documents

Novel potent and efficacious nonpeptidic urotensin II receptor agonists

Six different series of nonpeptidic urotensin II receptor agonists have been synthesized and evaluated for their agonistic activity in a cell-based assay (R-SAT). The compounds are ring-opened analogues of the isochromanone-based agonist AC-7954 with different functionalities constituting the linker between the two aromatic ring moieties. Several of the compounds are highly potent and efficacious, with N-[1-(4-chlorophenyl)-3-(dimethylamino)- propyl]-4-phenylbenzamide oxalate (5d) being the most potent. The pure enantiomers of 5d were obtained from the corresponding diastereomeric amides. It was shown by a combination of X-ray crystallography and chemical correlation that the activity resides in the S-enantiomer of 5d (pEC50 7.49).