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3,5-Dichloro-4-methoxy-pyridazine is a chemical compound with the molecular formula C6H4Cl2N2O. It is a derivative of pyridazine, a heterocyclic compound consisting of a six-membered ring with two nitrogen atoms. The compound features two chlorine atoms at the 3rd and 5th positions and a methoxy group at the 4th position. This organic compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through chemical reactions involving pyridazine and halogenated compounds, and its properties can be further explored for potential uses in the development of new drugs and pesticides.

2288-74-6

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2288-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2288-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2288-74:
(6*2)+(5*2)+(4*8)+(3*8)+(2*7)+(1*4)=96
96 % 10 = 6
So 2288-74-6 is a valid CAS Registry Number.

2288-74-6SDS

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 3,5-dichloro-4-methoxypyridazine

1.2 Other means of identification

Product number -
Other names Pyridazine,3,5-dichloro-4-methoxy

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:2288-74-6 SDS

2288-74-6Relevant academic research and scientific papers

TRIAZOLE-PYRIDINYL SUBSTITUTED AZACYCLOHEXYL ACETIC ACID COMPOUNDS AS LPA RECEPTOR ANTAGONISTS

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Paragraph 0446, (2022/02/28)

This application relates to novel substituted azacyclohexyl acetic acid compounds, their manufacture, pharmaceutical compositions comprising them, and their use as medicaments for treating a disease associated with dysregulation of lysophosphatidic acid receptors (LPA).

Studies on Syntheses and Reaction of Methoxypyridazines. I. Methoxylation of 3,4,5-Trichloropyridazine

Nagashima, Hiromu,Oda, Hirohisa,Hida, Jun-Ichi,Kaji, Kenji

, p. 421 - 424 (2007/10/02)

The reaction of 3,4,5-trichloropyridazine (1) with 1 eq amount of NaOMe resulted in the formation of three dichloromonomethoxypyridazines (2, 3-OMe; 3, 4-OMe; 4, 5-OMe) in the ratio of 1:3:6.The 4-OMe compound 3 was isolated from the reaction mixture and the 3-OMe compound 2 was syntesizsed independently.Further methoxylation of 2, 3 and 4 was also investigated in order to prepare various substituted pyrazines.Keywords - 3,4,5-trichloropyridazine; methoxylation; dichloromonomethoxypyridazine; monochlorodimethoxypyridazine; pyridazinone; 3,4,5-trimethoxypyridazine

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