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5-Amino-1-methyl-1H-pyrazole-3-carboxylic acid ethyl ester is a chemical compound that belongs to the class of organic compounds known as pyrazoles. These are polycyclic aromatic compounds with a five-membered ring consisting of three carbon atoms and two nitrogen atoms. 5-Amino-1-methyl-1H-pyrazole-3-carboxylic acid ethyl ester has a molecular formula of C7H11N3O2 and is systematically named as ethyl 1-methyl-5-amino-1H-pyrazole-3-carboxylate. Its structure, featuring amino, methyl, and carboxylate groups, contributes to its reactivity and intrinsic properties, making it a valuable compound in chemical research and synthesis.

70500-80-0

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70500-80-0 Usage

Uses

Used in Chemical Research:
5-Amino-1-methyl-1H-pyrazole-3-carboxylic acid ethyl ester is used as a research compound for its unique structure and reactivity. It is particularly valuable in the study of pyrazole chemistry and the development of new synthetic pathways.
Used in Synthesis:
5-Amino-1-methyl-1H-pyrazole-3-carboxylic acid ethyl ester is used as a synthetic intermediate in the preparation of various complex organic molecules. Its versatile functional groups allow for a wide range of chemical reactions, making it a useful building block in organic synthesis.
Used in Pharmaceutical Industry:
5-Amino-1-methyl-1H-pyrazole-3-carboxylic acid ethyl ester is used as a starting material in the synthesis of pharmaceutical compounds. Its structural features can be exploited to design and develop new drugs with potential therapeutic applications.
Used in Material Science:
5-Amino-1-methyl-1H-pyrazole-3-carboxylic acid ethyl ester is used as a component in the development of new materials with specific properties. Its incorporation into polymers or other materials can lead to novel materials with improved characteristics for various applications.
Used in Agrochemical Industry:
5-Amino-1-methyl-1H-pyrazole-3-carboxylic acid ethyl ester is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and structural features can be utilized to create new compounds with enhanced efficacy and selectivity in agricultural applications.

Check Digit Verification of cas no

The CAS Registry Mumber 70500-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,0 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70500-80:
(7*7)+(6*0)+(5*5)+(4*0)+(3*0)+(2*8)+(1*0)=90
90 % 10 = 0
So 70500-80-0 is a valid CAS Registry Number.

70500-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-amino-1-methyl-1H-pyrazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 5-amino-1-methylpyrazole-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:70500-80-0 SDS

70500-80-0Downstream Products

70500-80-0Relevant academic research and scientific papers

POLYCYCLIC COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF RAPIDLY ACCELERATED FIBROSARCOMA POLYPEPTIDES

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Paragraph 2097; 2098, (2020/03/29)

The present disclosure relates to bifunctional compounds, ULM— L—PTM, which find utility as modulators of Rapidly Accelerated Fibrosarcoma (RAF, such as c-RAF, A- RAF and/or B-RAF; the target protein). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a Von Hippel-Lindau, cereblon, Inhibitors of Apotosis Proteins or mouse double-minute homolog 2 ligand which binds to the respective E3 ubiquitin ligase and on the other end a moiety which binds the target protein RAF, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation or accumulation of the target protein, or the constitutive activation of the target protein, are treated or prevented with compounds and compositions of the present disclosure.

NOVEL THIAZOLOPYRAZOLES AND METHODS OF THEIR USE

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Page/Page column 55, (2008/06/13)

This invention concerns novel thiazolopyrazole compounds of formula (I) and compositions comprising them. Methods of using these compounds for the treatment, prevention and management of various diseases and disorders are also encompassed by the invention.

4,7-dihydropyrazolo(3,4-b) pyridine derivatives

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, (2008/06/13)

Novel Ca-blockers, 4,7-dihydropyrazolo[3,4-b]pyridine derivatives having potent antihypertensive and coronary vasodilating actions and useful in treatment for diseases in circulatory system, but without systole inhibitory action.

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