59774-06-0

Basic information

• Product Name: α-bromohexanophenone
• Synonyms: α-bromohexanophenone
• CAS NO: 59774-06-0
• Molecular Weight: 255.155
• Mol File: 59774-06-0.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 98 °C(Press: 0.3 Torr)
• Density: 1.272±0.06 g/cm3(Predicted)
• CAS DataBase Reference: α-bromohexanophenone(CAS DataBase Reference)
• NIST Chemistry Reference: α-bromohexanophenone(59774-06-0)
• EPA Substance Registry System: α-bromohexanophenone(59774-06-0)

Safety Data

• Hazardous Substances Data: 59774-06-0(Hazardous Substances Data)

Usage

Uses

This product is sold as designer drug on the illicit drug market.

Upstream product

• 71-43-2 benzene 
• 4471-05-0 1-phenylhexan-1-ol 
• 54971-26-5 2-bromohexanoyl bromide 
• 93-58-3 benzoic acid methyl ester 
• 13320-56-4 1,1-dibromopentane 
• 942-92-7 caprophenone 
• 142-61-0 Hexanoyl chloride 
• 1077-16-3 hexylbenzene 

Downstream Products

• 100615-25-6 5-butyl-4-phenyl-oxazol-2-ylamine 
• 100615-17-6 4-butyl-5-phenyl-1,3-dihydro-imidazol-2-one 
• 103039-52-7 2-Hydroxy-1-phenyl-1-hexanone 
• 59774-08-2 1-benzoylpentyl dimethylsulphonium tetrafluoroborate 
• 5423-45-0 1-phenyl-2-(piperidine-1-yl)hexan-1-one hydrochloride 
• 162048-68-2 Dithiocarbonic acid S-(1-benzoyl-pentyl) ester O-ethyl ester 
• 345207-68-3 tetrahydro-3-butyl-2-hydroxy-4-(2-hydroxyethyl)-2-phenyl-2H-1,4-oxazine 

Relevant articles and documents

Regiospecific Synthesis of α-Haloketones using α-Haloalkyllithium Reagents

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Cathinone Derivatives, Pharmaceutical Formulations, and Methods

Compounds, such as cathinone derivatives, and pharmaceutical formulations that include the compounds. The compounds may have a first selectivity for a first receptor subtype that is at least 10 times greater than a second selectivity for a second receptor subtype from the same class of receptors. Methods of treating patients, which may include administering to a patient a pharmaceutical formulation that includes a compound, such as a cathinone derivative.

2-Amino-4-arylthiazoles through One-Pot Transformation of Alkylarenes with NBS and Thioureas

Treatment of alkylarenes with N-bromosuccinimide in a mixture of ethyl acetate and water at 60 °C, a mixture of acetonitrile and water at 80 °C, or a mixture of diethyl carbonate and water under irradiation with a tungsten lamp, followed by a reaction with thioureas or arenethioamides provided the corresponding 2-amino- 4-arylthiazoles or 2,4-diarylthiazoles in good to moderate yields, respectively, in one pot. The present reaction is an efficient one-pot transformation method of alkylarenes into 2-amino-4-arylthiazoles and 2,4-diarylthiazoles directly under mild and transition-metal-free conditions.