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METHYL 4-CHLORO-6-OXO-1-[3-(TRIFLUOROMETHYL)PHENYL]-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLATE is a complex organic chemical compound characterized by its molecular formula C14H8ClF3N2O3. It incorporates chlorine, fluorine, and nitrogen atoms within its structure, indicating a potential for diverse reactivity and applications. As a synthetic compound, its specific properties such as physical state, boiling and melting points, density, and solubility are contingent upon its synthesis and subsequent testing. METHYL 4-CHLORO-6-OXO-1-[3-(TRIFLUOROMETHYL)PHENYL]-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLATE is likely utilized in scientific research or industrial applications, possibly in pharmaceutical development or the creation of advanced materials. Due to its chemical composition, it is essential to handle METHYL 4-CHLORO-6-OXO-1-[3-(TRIFLUOROMETHYL)PHENYL]-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLATE with caution to mitigate any risks associated with its reactivity or the byproducts formed during its use.

129109-18-8

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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

129109-18-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-chloro-6-oxo-1-[3-(trifluoromethyl)phenyl]pyridazine-3-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 4-chloro-1,6-dihydro-6-oxo-1-[3-(trifluoromethyl)phenyl]pyridazin-3-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:129109-18-8 SDS

129109-18-8Relevant academic research and scientific papers

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

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