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121582-55-6

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121582-55-6 Usage

General Description

Methyl 4-hydroxy-6-oxo-1-[3-(trifluoromethyl)phenyl]-1,6-dihydro-3-pyridazinecarboxylate is a chemical compound with potential pharmacological properties. It belongs to the class of pyridazinecarboxylates and contains a trifluoromethyl group and a hydroxyketo functional group. This chemical may have applications in medicinal chemistry research, particularly in the development of new drugs for various purposes. Further studies and investigations are necessary to fully understand the potential uses and effects of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 121582-55-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,5,8 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 121582-55:
(8*1)+(7*2)+(6*1)+(5*5)+(4*8)+(3*2)+(2*5)+(1*5)=106
106 % 10 = 6
So 121582-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H9F3N2O4/c1-22-12(21)11-9(19)6-10(20)18(17-11)8-4-2-3-7(5-8)13(14,15)16/h2-6,19H,1H3

121582-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-hydroxy-6-oxo-1-[3-(trifluoromethyl)-phenyl]-1,6-dihydro-3-pyridazinecarboxylate

1.2 Other means of identification

Product number -
Other names methyl 4-hydroxy-6-oxo-1-[3-(trifluoromethyl)phenyl]pyridazine-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:121582-55-6 SDS

121582-55-6Relevant articles and documents

Pyridazinone compound and use thereof

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Paragraph 0068; 0129-0132, (2017/10/13)

The present invention provides a pyridazinone compound of formula (I) and its use as a plant induced-resistance activator. In the formula, R1-R5 are independently selected from: hydrogen, C1-C6 alkyl, C1-C6 alkoxy, halogen, C1-C6 haloalkyl, C1-C6 haloalkoxy, nitro, amino, CN, NCO, NCS, carboxyl, C1-C3 alkoxy formacyl, and C1-C3 amido; X is selected from oxygen, sulfur and nitrogen; R6 is H, optionally substituted C1-C3 alkyl, optionally substituted phenyl, and 5-10 member heteroaryl; and R7 is H, optionally substituted C1-C3 alkyl and optionally substituted phenyl.

Pyridazines with Heteroatom Substituents in Position 3 and 5. 3) 2-Aryl-5-hydroxypyridazin-3(2H)-ones as Potential Herbicides: Synthesis and Some Reactions

Schober, Bernt D.,Megyeri, Gabor,Kappe, Thomas

, p. 169 - 176 (2007/10/02)

The coupling of dimethyl acetonedicarboxylate 1 with a variety of aryldiazonium salts 2a-i produces the hydrazones 3a-i which can be cyclized in boiling dichlorobenzene to yield the pyridazone esters 4a-i, or in sodium hydroxide solution to give the pyrid

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