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1,2-Propanedione, 3-bromo-1-(4-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29680-63-5

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29680-63-5 Usage

Molecular structure

A brominated derivative of fluoroarene

Physical state

Clear, colorless to pale yellow liquid

Odor

Pungent smell

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Hazardous properties

Toxic and irritant

Safety precautions

Handle with care due to its hazardous nature

Check Digit Verification of cas no

The CAS Registry Mumber 29680-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,8 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29680-63:
(7*2)+(6*9)+(5*6)+(4*8)+(3*0)+(2*6)+(1*3)=145
145 % 10 = 5
So 29680-63-5 is a valid CAS Registry Number.

29680-63-5Relevant academic research and scientific papers

LXR MODULATORS

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Page/Page column 101, (2014/09/29)

The present invention provides compounds of Formula I: and pharmaceutically acceptable salts or solvates thereof, as modulators of liver X receptors (LXR), compositions comprising any of such novel compounds, methods of using these compounds or compositions as medicaments for prevention or treatment of diseases or disorders related to liver X receptor (LXR), as well as methods of preparing these LXR modulators and using them in the manufacture of medicaments.

Quinoxalines. Part 13: Synthesis and mass spectrometric study of aryloxymethylquinoxalines and benzo[b]furylquinoxalines

Starke, Ines,Sarodnick, Gerhard,Ovcharenko, Vladimir V.,Pihlaja, Kalevi,Kleinpeter, Erich

, p. 6063 - 6078 (2007/10/03)

A series of new aryloxymethylquinoxalines, benzo[b]- and naphtho[2,1-b]furylquinoxalines, possessing potential biological activity, was prepared, characterized by IR and NMR spectroscopy and their electron ionization (EI) mass spectra studied in detail. The aryloxymethylquinoxalines were obtained by reacting halogenomethylquinoxalines with bifunctional O-nucleophiles. The benzo[b]furylquinoxalines and naphtho[2,1-b] furylquinoxalines were prepared via two routes, which differed in the order of the two cyclization steps involved in the syntheses. The composition of the ions obtained by EI mass spectrometry were determined by accurate mass measurements and the fragmentation pathways clarified by B/E linked scans and collision induced dissociation. The mass spectrometric behaviour of the compounds studied as to the possible loss of OH· radicals proved to be very characteristic.

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