4316-97-6

Usage

Chemical Properties

White Solid

InChI:InChI=1/C5H4Cl2N2/c1-3-4(6)8-2-9-5(3)7/h2H,1H3

Upstream product

• 63447-38-1 5-methyl-1H-pyrimidine-4,6-dione 
• 18337-63-8 4,6-Dihydroxy-5-methyl-pyrimidin 

Downstream Products

• 2036-41-1 5-methylpyrimidine 
• 14394-56-0 6-chloro-5-methylpyrimidin-4-amine 
• 960297-56-7 4-chloro-5-methyl-6-(2-methylbenzyl)pyrimidine 
• 960299-06-3 4-chloro-6-methoxy-5-methylpyrimidine 
• 17758-50-8 5-methyl-pyrimidine 1-oxide 
• 940871-42-1 1-(2-(6-chloro-5-methylpyrimidin-4-yloxy)benzyl)-3-(3-t-butyl-1-p-tolyl-1 H-pyrazol-5-yl)urea 
• 67434-65-5 4-chloro-5,6-dimethylpyrimidine 
• 930093-72-4 4-chloro-5-methyl-6-[(2-methylpyridin-3-yl)oxy]pyrimidine 
• 99852-10-5 4-chloro-5-methyl-6-phenyl-pyrimidine 
• 1373880-83-1 4-chloro-5-methyl-6-(2-methylphenyl)pyrimidine 
• 1373880-84-2 5-methyl-6-(2-methylphenyl)-4-phenylpyrimidine 
• 1426320-75-3 4-chloro-6-(3,4-dichloro-phenyl)-5-methyl-pyrimidine 
• 1426320-76-4 6-(3,4-dichloro-phenyl)-5-methyl-pyrimidine-4-carboxylic acid methyl ester 
• 1449202-70-3 6-chloro-N-[2-[2-fluoro-4-[[4-(trifluoromethyl)-2-pyridyl]oxy]phenyl]ethyl]-5-methyl-pyrimidin-4-amine 

Relevant academic research and scientific papers

Processes for preparing aromatic ethers

The present invention relates to processes for preparing aromatic ether compounds that are modulators of glucose metabolism and therefore useful in the treatment of metabolic disorders such as diabetes and obesity.

PYRIMIDINE DERIVATIVES AND HERBICIDES CONTAINING THE SAME

The present invention provides a pyrimidine derivative represented by the formula: wherein R1p and R1q are the same or different, and each represents (1)hydrogen, (2)halogen, (3) a C1-6alkyl group which may be substituted or (4) a C1-6alkoxy group, and so on, R2 is halogen, a C1-6alkyl group, cyano group, and so on, Ar is a phenyl group which may be substituted or is a condensed hetero ring which may be substituted, which has excellent selective herbicidal activity, and a herbicide containing the derivative.