71126-19-7

Upstream product

• 88-65-3 2-bromobenzoic-acid 
• 74-85-1 ethene 
• 7154-66-7 2-bromobenzoic acid chloride 

Downstream Products

• 71132-66-6 1-(2-bromophenyl)-3-(N,N-dimethylamino)-1-propanone 
• 71095-38-0 1-Amino-2-(2-bromo-phenyl)-4-dibenzylamino-butan-2-ol 
• 71095-39-1 1-Amino-2-(2-bromo-phenyl)-4-diethylamino-butan-2-ol 
• 71132-65-5 1-Amino-2-(2-bromo-phenyl)-4-dimethylamino-butan-2-ol 
• 125114-77-4 7-bromo-2,3-dihydro-1H-inden-1-one 
• 71095-46-0 2'-Brom-3-N,N-dibenzylaminopropiophenon 

Relevant academic research and scientific papers

Metallocene compound, catalyst component for olefin polymerization and catalyst for olefin polymerization containing the same, and method for producing olefin polymer using catalyst for olefin polymerization

The metallocene compound represented by the following general formula (1): (the numerals and signs in the general formula (1) are as described in the description).

METALLOCENE COMPOUNDS, OLEFIN POLYMERIZATION CATALYST COMPONENTS AND OLEFIN POLYMERIZATION CATALYSTS CONTAINING THE SAME, AND OLEFIN POLYMER PRODUCTION METHODS USING OLEFIN POLYMERIZATION CATALYSTS

PROBLEM TO BE SOLVED: To provide: metallocene compounds allowing production of ethylenic polymers with sufficient numbers of long chain branches having sufficient length introduced to improve molding processability of metallocene polyethylene; olefin polymerization catalyst components and olefin polymerization catalysts containing the compounds; and methods of producing olefin polymers (particularly ethylenic polymers) using those olefin polymerization catalysts. SOLUTION: The present invention provides, e.g., metallocene compounds represented by the general formula (1) in the figure. COPYRIGHT: (C)2015,JPO&INPIT

THERAPEUTIC FLUOROETHYLCYANO GUANIDINES

Disclosed herein is compound having a formula as described herein. Therapeutic methods, compositions, and medicaments related thereto are also disclosed.

A Convenient Synthesis of 7-Halo-1-indanones and 8-Halo-1-tetralones

A regioselective oxidation of N-indan-4-yl-acetamide or N-(5,6,7,8-tetrahydronaphthalen-1-yl)acetamide with potassium permanganate followed by acidic hydrolysis gave 7-aminoindan-1-one or 8-aminotetral-1-one in good yield. The amino ketones were converted to the corresponding 7-haloindanone or the 8-halotetralone. Another method to prepare 7-haloindan-1-ones was completed by a cyclization of 3-chloro-1-(2-halophenyl)propan-1-one under Friedel-Crafts conditions to produce the product in gram quantity.