91606-60-9 Usage
General Description
4-methyl-6-(trifluoromethyl)-2-pyrimidinol is a chemical compound with the molecular formula C6H6F3NO. It is commonly known as SALTDATA: FREE and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. 4-methyl-6-(trifluoromethyl)-2-pyrimidinol(SALTDATA: FREE) is a white solid that is sparingly soluble in water but soluble in organic solvents. It is also known for its potential use as a fungicide and pesticide due to its inhibitory effects on certain enzymes in plants. Additionally, it is classified as a trifluoromethylpyrimidine and is considered to be a potential toxicant. Its main applications include its use in medicinal chemistry and the production of crop protection products.
Check Digit Verification of cas no
The CAS Registry Mumber 91606-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,0 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91606-60:
(7*9)+(6*1)+(5*6)+(4*0)+(3*6)+(2*6)+(1*0)=129
129 % 10 = 9
So 91606-60-9 is a valid CAS Registry Number.
91606-60-9Relevant articles and documents
COMPOUNDS USEFUL AS CHEMOKINE RECEPTOR ANTAGONISTS
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Page/Page column 88, (2008/06/13)
The present invention relates to compounds useful as Chemokine Receptor antagonists. Compounds of general formula I are provided: or pharmaceutically acceptable salts thereof. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compounds and compositions for the inhibition of Chemokine Receptors and also for the treatment of various diseases, conditions, or disorders, including acute or chronic inflammatory disease, cancer or osteolytic bone disorders.
Synthesis of fluorinated heterocycles
Sloop, Joseph C.,Bumgardner, Carl L.,Loehle, W. David
, p. 135 - 147 (2007/10/03)
Selected 1,3-diketones having a trifluoromethyl group and/or a fluorine in the 2-position were condensed with aromatic hydrazines, hydroxylamine, urea, thiourea, guanidine, and substituted anilines producing pyrazoles, isoxazoles, pyrimidines, and quinolines, respectively, in yields ranging from 27 to 87%.
