66549-34-6 Usage
General Description
3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE is a chemical compound with the molecular formula C10H8ClN3. It is a pyridazine derivative with a chlorine and a 3-methylphenyl group attached to the 3 and 6 positions, respectively. 3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE has a wide range of applications in the pharmaceutical and agrochemical industries, where it is used as a building block for the synthesis of various biologically active compounds. Its unique structure and reactivity make it a valuable intermediate for the production of drugs, pesticides, and other fine chemicals. Additionally, it may also have potential uses in research and development for the creation of new chemical entities with desirable properties.
Check Digit Verification of cas no
The CAS Registry Mumber 66549-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,4 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66549-34:
(7*6)+(6*6)+(5*5)+(4*4)+(3*9)+(2*3)+(1*4)=156
156 % 10 = 6
So 66549-34-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H9ClN2/c1-8-3-2-4-9(7-8)10-5-6-11(12)14-13-10/h2-7H,1H3
66549-34-6Relevant articles and documents
Pd-catalyzed chemoselective cross-coupling reaction of triaryl- or triheteroarylbismuth compounds with 3,6-dihalopyridazines
Urgin, Karene,Aube, Christophe,Pipelier, Muriel,Blot, Virginie,Thobie-Gautier, Christine,Sengmany, Stephane,Lebreton, Jacques,Leonel, Eric,Dubreuil, Didier,Condon, Sylvie
supporting information, p. 117 - 124 (2013/02/22)
The cross-coupling reactions of 3,6-dihalopyridazines with triaryl- or triheteroarylbismuth compounds were performed under palladium catalysis. The reaction was highly chemoselective, affording functionalized aryl- or heteroarylpyridazinyl chlorides in moderate to good yields. The cross-coupling reactions of 3,6-dihalopyridazines with triaryl- or triheteroarylbismuth compounds were performed under palladium catalysis. The reaction was highly chemoselective, affording functionalized aryl- or heteroarylpyridazinyl chlorides in moderate to good yields. Copyright
