76970-14-4 Usage
General Description
3-Chloro-6-(3-methoxyphenyl)-pyridazine is a chemical compound with the molecular formula C10H8ClN3O. It is a pyridazine derivative and contains a chlorine atom, a methoxy group, and a phenyl ring. It is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. 3-CHLORO-6-(3-METHOXYPHENYL)-PYRIDAZINE has potential applications in the field of medicinal chemistry and drug development due to its structural features and reactivity. Its properties and reactivity make it an important building block in the preparation of various biologically active molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 76970-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76970-14:
(7*7)+(6*6)+(5*9)+(4*7)+(3*0)+(2*1)+(1*4)=164
164 % 10 = 4
So 76970-14-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H9ClN2O/c1-15-9-4-2-3-8(7-9)10-5-6-11(12)14-13-10/h2-7H,1H3
76970-14-4Relevant 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