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Ethyl 3-methoxy-1-methyl-1H-pyrazole-4-carboxylate is an organic compound that serves as a key intermediate in the synthesis of various chemical compounds. It is characterized by its pyrazole ring structure, which is a five-membered heterocyclic ring containing nitrogen atoms, and an ester functional group. ethyl 3-methoxy-1-methyl-1H-pyrazole-4-carboxylate is known for its potential applications in the development of herbicidal agents and other chemical products.

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  • 103626-04-6 Structure
  • Basic information

    1. Product Name: ethyl 3-methoxy-1-methyl-1H-pyrazole-4-carboxylate
    2. Synonyms: ethyl 3-methoxy-1-methyl-1H-pyrazole-4-carboxylate;ethyl 3-methoxy-1-methyl-1H-pyrazol-4-carboxylate;3-Methoxy-1-Methyl-1H-Pyrazole-4-Carboxylic Acid Ethyl Ester;1H-Pyrazole-4-carboxylic acid, 3-methoxy-1-methyl-, ethyl ester;3-Methoxy-1-Methyl-1H-Pyrazole-4-Carboxylic Acid Ethyl Ester(WX618388)
    3. CAS NO:103626-04-6
    4. Molecular Formula: C8H12N2O3
    5. Molecular Weight: 184.19248
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103626-04-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 289.6±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.18±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -0.43±0.10(Predicted)
    10. CAS DataBase Reference: ethyl 3-methoxy-1-methyl-1H-pyrazole-4-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: ethyl 3-methoxy-1-methyl-1H-pyrazole-4-carboxylate(103626-04-6)
    12. EPA Substance Registry System: ethyl 3-methoxy-1-methyl-1H-pyrazole-4-carboxylate(103626-04-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 103626-04-6(Hazardous Substances Data)

103626-04-6 Usage

Uses

Used in Herbicide Industry:
Ethyl 3-methoxy-1-methyl-1H-pyrazole-4-carboxylate is used as a reagent for the preparation of pyrazole-4-carboxamide derivatives with herbicidal activity. These derivatives are effective in controlling the growth of various weeds, making them valuable for agricultural and horticultural applications. ethyl 3-methoxy-1-methyl-1H-pyrazole-4-carboxylate's ability to form herbicidal agents contributes to its significance in the development of new and improved weed control products.

Check Digit Verification of cas no

The CAS Registry Mumber 103626-04-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,2 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 103626-04:
(8*1)+(7*0)+(6*3)+(5*6)+(4*2)+(3*6)+(2*0)+(1*4)=86
86 % 10 = 6
So 103626-04-6 is a valid CAS Registry Number.

103626-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-methoxy-1-methylpyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole-4-carboxylic acid,3-methoxy-1-methyl-,ethyl 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:103626-04-6 SDS

103626-04-6Relevant articles and documents

USE OF MORPHINAN DERIVATIVES FOR TREATMENT OF OPIOID RECEPTOR AGONIST-RELATED DISEASES

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, (2019/08/01)

The present invention relates to a pharmaceutical composition comprising a morphinan derivative that exhibits an opioid δ receptor agonist activity. By administering the pharmaceutical composition provided by the present invention, opioid δ receptor-related diseases (for example, headache) can be treated or prevented.

MORPHINAN DERIVATIVE

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Paragraph 0222; 0223, (2018/03/02)

A morphinan derivative represented by the following general formula (I): (wherein R1 represents hydrogen, C1-10 alkyl, cycloalkylalkyl where the cycloalkyl moiety has 3 to 6 carbon atoms, and the alkylene moiety has 1 to 5 carbon atoms, etc., R2 represents heterocyclic ring containing 1 to 4 heteroatoms selected from N, O and S and at least one carbon atom as ring-constituting atoms, containing at least one set of adjacent ring-constituting atoms bound by a double bond, and further substituted with at least one oxo group, Y binds to a carbon atom as a ring-constituting atom of R2, R3, R4, and R5 represent hydrogen; hydroxy, etc., R6a and R6b represent hydrogen, etc., R7 and R8 represent hydrogen, etc., R9 and R10, which are the same or different, represent hydrogen, etc., X represents O or CH2, and Y represents C(=O)), a tautomer or stereoisomer of the compound, or a pharmaceutically acceptable salt thereof, or a solvate thereof is used as an anxiolytic drug, antidepressant, etc.

1,3-Dimethylbutyl carboxanilides for controlling undesirable micro-organisms

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, (2008/06/13)

This invention relates to novel 1,3-dimethylbutylcarboxanilides of the formula (I) in which A, R1 and R2 are as defined in the disclosure, to a plurality of processes for preparing these compounds and their use for controlling unwant

1,3-DIMETHYLBUTYL CARBOXANILIDES FOR CONTROLLING UNDESIRABLE MICRO-ORGANISMS

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Page/Page column 44, (2010/02/11)

The invention relates to novel 1,3-dimethylbutyl carboxanilides of formula (I), in which A, R1 and R2 are defined as cited in the description, to several methods for producing said substances, to their use for controlling undesirable

Synthesis and hypoglycemic evaluation of substituted pyrazole-4-carboxylic acids.

Cottineau, Bertrand,Toto, Patrick,Marot, Christophe,Pipaud, Aline,Chenault, Jacques

, p. 2105 - 2108 (2007/10/03)

The synthesis and in vivo activities of a series of substituted pyrazole-4-carboxylic acids as hypoglycemic agents are described. Modelization of some potent compounds, comparatively to the metformine, presents certain analogies permitting to predict the design of some novel antidiabetic drugs.

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