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METHYL 6-CHLORO-4-METHOXYPYRIDAZINE-3-CARBOXYLATE is a pyridazine derivative with the chemical formula C9H8ClN2O3. It features a methyl ester group, a chlorine atom, and a methoxy group, which contribute to its unique structure and reactivity. This chemical compound holds potential in the fields of organic synthesis and medicinal chemistry, making it a valuable asset for research and development within the pharmaceutical industry.

679405-85-7

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679405-85-7 Usage

Uses

Used in Organic Synthesis:
METHYL 6-CHLORO-4-METHOXYPYRIDAZINE-3-CARBOXYLATE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, facilitating the creation of new molecules with specific properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, METHYL 6-CHLORO-4-METHOXYPYRIDAZINE-3-CARBOXYLATE is utilized as a building block for the development of pharmaceutical agents. Its reactivity and functional groups enable the design of novel drug candidates with potential therapeutic applications.
Used in Pharmaceutical Research and Development:
METHYL 6-CHLORO-4-METHOXYPYRIDAZINE-3-CARBOXYLATE plays a crucial role in pharmaceutical research and development. It is employed in the exploration of new drug targets and the optimization of lead compounds, contributing to the advancement of innovative treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 679405-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,9,4,0 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 679405-85:
(8*6)+(7*7)+(6*9)+(5*4)+(4*0)+(3*5)+(2*8)+(1*5)=207
207 % 10 = 7
So 679405-85-7 is a valid CAS Registry Number.

679405-85-7SDS

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 6-chloro-4-methoxypyridazine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 3-PYRIDAZINECARBOXYLIC ACID,6-CHLORO-4-METHOXY-,METHYL ESTER

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:679405-85-7 SDS

679405-85-7Relevant academic research and scientific papers

1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS

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Paragraph 00189, (2021/08/06)

Compounds according to formula I or II are useful as agonists of Toll-like receptor 7 (TLR7). Such compounds can be used in cancer treatment, especially in combination with an anti-cancer immunotherapy agent, or as a vaccine adjuvant.

C5A RECEPTOR MODULATORS

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Page/Page column 82, (2019/08/08)

The present invention relates to derivatives of formula (I) wherein ring A, X, Y, Z, R1, R2, R3 and R4 are as described in the description, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as C5a receptor modulators.

Imidazol-1-ylmethyl pyridazine derivatives

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Page 18, (2010/02/06)

The invention provides imidazol-1-ylmethyl pyridazine derivatives of the formula: 1 that bind to GABAA receptors. In the above formula, R1, R2 R3, R4, R5, R6 and Ar are defined herein. Such compounds may be used to modulate ligand binding to GABAA receptors in vivo or in vitro, and are particularly useful in the treatment of a variety of central nervous system (CNS) disorders in humans, domesticated companion animals, and livestock animals. Compounds provided herein may be administered alone or in combination with one or more other CNS agents to potentiate the effects of the other CNS agent(s). Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for detecting GABAA receptors (e.g., receptor localization studies).

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