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1H-Pyrazole-3-carboxaldehyde, 5-(methylthio)(9CI), also known as 5-(methylthio)-1H-pyrazole-3-carbaldehyde, is a chemical compound with the molecular formula C6H6N2OS. It is a derivative of pyrazole, featuring a five-membered ring with two nitrogen atoms. The presence of a carboxaldehyde group and a methylthio substituent endows 1H-Pyrazole-3-carboxaldehyde, 5-(methylthio)- (9CI) with unique chemical properties, making it valuable in synthetic organic chemistry and pharmaceutical research. It also holds potential for applications in the development of agrochemicals and pharmaceutical products, showcasing its versatility across different industries.

569657-30-3

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569657-30-3 Usage

Uses

Used in Synthetic Organic Chemistry:
1H-Pyrazole-3-carboxaldehyde, 5-(methylthio)(9CI) is used as a key intermediate in the synthesis of various organic compounds due to its unique chemical properties. Its reactivity allows for the formation of new bonds and the creation of diverse molecular structures, which is crucial in the development of novel organic materials.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1H-Pyrazole-3-carboxaldehyde, 5-(methylthio)(9CI) serves as a building block for the design and synthesis of potential drug candidates. Its unique structure and functional groups can be leveraged to create new molecules with therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Development:
1H-Pyrazole-3-carboxaldehyde, 5-(methylthio)(9CI) is utilized in the development of agrochemicals, such as pesticides and herbicides. Its chemical properties make it a promising candidate for the creation of effective and environmentally friendly agricultural products.
Used in the Development of Pharmaceutical Products:
1H-Pyrazole-3-carboxaldehyde, 5-(methylthio)(9CI) is employed in the pharmaceutical sector for the development of new drugs. Its unique structure and functional groups can be exploited to design molecules with specific therapeutic targets, potentially leading to the discovery of innovative treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 569657-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,9,6,5 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 569657-30:
(8*5)+(7*6)+(6*9)+(5*6)+(4*5)+(3*7)+(2*3)+(1*0)=213
213 % 10 = 3
So 569657-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2OS/c1-9-5-2-4(3-8)6-7-5/h2-3H,1H3,(H,6,7)

569657-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylsulfanyl-1H-pyrazole-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names -

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

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More Details:569657-30-3 SDS

569657-30-3Downstream Products

569657-30-3Relevant academic research and scientific papers

1-Bis(methoxy)-4-bis(methylthio)-3-buten-2-one: Useful three carbon synthon for synthesis of five and six membered heterocycles with masked (or unmasked) aldehyde functionality

Mahata, Pranab K.,Syam Kumar,Sriram,Ila,Junjappa

, p. 2631 - 2639 (2007/10/03)

1-Bis(methoxy)-4-bis(methylthio)-3-buten-2-one has been shown to be a useful three carbon synthon for efficient regiospecific synthesis of a variety of five (pyrazole and isoxazole) and six membered (pyrimidines, pyridone and pyridines) heterocycles with masked (or unmasked) aldehyde functionality by cyclocondensation with bifunctional heteronucleophiles such as hydrazine, hydroxylamine, guanidine, thiourea, cyanoacetamide and substituted β-lithioaminoacrylonitriles. Reaction of 1-bis(methoxy)-4-bis(methylthio)-3-buten-2-one with methylene iodide and Zn-Cu couple under Simmons-Smith reaction conditions afforded 2-(methylthio)thiophene-4-aldehyde in good yield, whereas cycloaromatization with thiophene-2- and 3-acetonitriles gave the corresponding substituted benzothiophene-4- and 7-aldehydes in good yields.

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