129109-18-8 Usage
Uses
Used in Pharmaceutical Development:
METHYL 4-CHLORO-6-OXO-1-[3-(TRIFLUOROMETHYL)PHENYL]-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLATE is used as a chemical intermediate for the synthesis of potential drug candidates. Its unique structure, containing chlorine and fluorine atoms, may contribute to the development of new pharmaceuticals with specific therapeutic properties.
Used in Advanced Material Synthesis:
In the field of materials science, METHYL 4-CHLORO-6-OXO-1-[3-(TRIFLUOROMETHYL)PHENYL]-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLATE is used as a building block for the creation of novel materials with tailored properties. Its incorporation into these materials could lead to advancements in various industries, such as electronics, where its chemical structure may impart specific electrical or optical characteristics.
Used in Scientific Research:
METHYL 4-CHLORO-6-OXO-1-[3-(TRIFLUOROMETHYL)PHENYL]-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLATE serves as a subject of study in chemical research, where its reactivity, stability, and interactions with other compounds are investigated. This research could lead to a better understanding of its potential applications and the development of safer handling protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 129109-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,0 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129109-18:
(8*1)+(7*2)+(6*9)+(5*1)+(4*0)+(3*9)+(2*1)+(1*8)=118
118 % 10 = 8
So 129109-18-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H8ClF3N2O3/c1-22-12(21)11-9(14)6-10(20)19(18-11)8-4-2-3-7(5-8)13(15,16)17/h2-6H,1H3
129109-18-8Relevant articles and documents
Pyridazines with Heteroatom Substituents in Position 3 and 5. 6. SN Reactions in Position 5 of 2-Aryl-5-hydroxypyridazin-3(2H)-ones
Schober, Berndt D.,Megyeri, Gabor,Kappe, Thomas
, p. 471 - 477 (2007/10/02)
The nucleophilic introduction of chloro- (2), azido- (4), (substituted) amino (3,6), mercapto (10) and hydrazino-groups (13) into 2-aryl-5-hydroxypyridazin-3(2H)-ones is described.The 5-aminopyridazin-3(2H)-one (6) also reacts with activated malonates 8 t