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3-Pyridazinecarboxylic acid, 6-amino-, methyl ester (6CI, 9CI), also known as 6-Aminonicotinic acid methyl ester, is a pyridazine derivative with the molecular formula C7H8N4O2. It is a chemical compound that has potential applications in pharmaceuticals and agrochemicals, and may be used as an intermediate in the synthesis of other organic compounds. With a molecular weight of 180.16 g/mol, 3-Pyridazinecarboxylicacid,6-amino-,methylester(6CI,9CI) is of interest to researchers and manufacturers in the chemical and pharmaceutical industries due to its unique properties and potential uses.

98140-96-6

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98140-96-6 Usage

Uses

Used in Pharmaceutical Industry:
3-Pyridazinecarboxylic acid, 6-amino-, methyl ester (6CI, 9CI) is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Pyridazinecarboxylic acid, 6-amino-, methyl ester (6CI, 9CI) may be used as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its potential applications in this field contribute to the development of more effective and environmentally friendly products.
Used in Organic Synthesis:
3-Pyridazinecarboxylic acid, 6-amino-, methyl ester (6CI, 9CI) is used as a key intermediate in the synthesis of other organic compounds. Its unique structure allows for various chemical reactions, making it a versatile building block in organic chemistry.
Used in Research and Development:
Due to its unique properties and potential applications, 3-Pyridazinecarboxylic acid, 6-amino-, methyl ester (6CI, 9CI) is used in research and development for exploring new chemical reactions, understanding its properties, and discovering new uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 98140-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,4 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 98140-96:
(7*9)+(6*8)+(5*1)+(4*4)+(3*0)+(2*9)+(1*6)=156
156 % 10 = 6
So 98140-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O2/c1-11-6(10)4-2-3-5(7)9-8-4/h2-3H,1H3,(H2,7,9)

98140-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 6-Aminopyridazine-3-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 3-aminopyridazine-6-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:98140-96-6 SDS

98140-96-6Relevant academic research and scientific papers

Development of a Scalable Synthesis of the Small Molecule TGFβR1 Inhibitor BMS-986260

Vetrichelvan, Muthalagu,Rakshit, Souvik,Chandrasekaran, Sathishkumar,Chinnakalai, Karthikeyan,Darne, Chetan Padmakar,Doddalingappa, Dyamanna,Gopikumar, Indasi,Gupta, Anuradha,Gupta, Arun Kumar,Karmakar, Ananta,Lakshminarasimhan, Thirumalai,Leahy, David K.,Palani, Senthil,Radhakrishnan, Vignesh,Rampulla, Richard,Savarimuthu, Antony,Subramanian, Varadharajan,Velaparthi, Upender,Warrier, Jayakumar,Eastgate, Martin D.,Borzilleri, Robert M.,Mathur, Arvind,Vaidyanathan, Rajappa

, p. 1310 - 1320 (2020/07/24)

A scalable route to the small molecule TGFβR1 inhibitor BMS-986260 (1) was developed. This alternative approach circumvented the purification of intermediates by column chromatography and provided access to multikilogram quantities of the key intermediate

NAMPT INHIBITORS

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Page/Page column 36, (2013/05/23)

Disclosed are compounds which inhibit the activity of NAMPT, compositions containing the compounds and methods of treating diseases during which NAMPT is expressed.

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