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5-Hydroxy-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carbaldehyde is a pyrazole derivative chemical compound characterized by the presence of an aldehyde, hydroxy, methyl, and trifluoromethyl group attached to a pyrazole ring. Its unique structure and reactivity make it a versatile component in various chemical reactions and synthesis processes. 5-Hydroxy-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carbaldehyde's potential applications in pharmaceutical research and drug development are attributed to its structural features and functional groups, which could contribute to the synthesis of biologically active compounds. The trifluoromethyl group further enhances its chemical and biological properties, making it a promising candidate for diverse applications.

179732-64-0

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179732-64-0 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
5-Hydroxy-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carbaldehyde is used as a building block in the synthesis of biologically active compounds due to its structural features and functional groups. Its incorporation into pharmaceutical compounds may enhance their chemical and biological properties, making it a valuable component in drug development.
Used in Chemical Reactions and Synthesis Processes:
5-Hydroxy-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carbaldehyde is used as a reactive component in various chemical reactions and synthesis processes. Its unique structure allows it to participate in a wide range of reactions, making it a versatile compound in the field of organic chemistry.
Used in Enhancing Chemical and Biological Properties:
The trifluoromethyl group present in 5-Hydroxy-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carbaldehyde is known to confer enhanced chemical and biological properties to the molecules it is incorporated into. This makes the compound a promising candidate for improving the performance of various chemical and pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 179732-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,7,3 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 179732-64:
(8*1)+(7*7)+(6*9)+(5*7)+(4*3)+(3*2)+(2*6)+(1*4)=180
180 % 10 = 0
So 179732-64-0 is a valid CAS Registry Number.

179732-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-3-oxo-5-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-HYDROXY-1-METHYL-3-TRIFLUOROMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE

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:179732-64-0 SDS

179732-64-0Downstream Products

179732-64-0Relevant academic research and scientific papers

PYRAZOLE DERIVATIVES AND PROCESS FOR THE PRODUCTION THEREOF

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Page/Page column 23, (2010/02/11)

The present invention provides pyrazole derivatives useful as production intermediates for isoxazoline derivatives having an excellent herbicidal effect and selectivity between crops and weeds as well as processes for producing the same. The pyrazole derivatives or pharmaceutically acceptable salts thereof which are inventive compounds are represented by the general formula [I] or a salt thereof: wherein R1 represents a C1 to C6 alkyl group, R2 represents a C1 to C3 haloalkyl group, R3 represents a hydrogen atom, a C1 to C3 alkyl group which may be substituted with one or more substituents selected from the following substituent group α, or a formyl group, R4 represents a hydrogen atom or a C1 to C3 haloalkyl group, provided that R4 represents a C1 to C3 haloalkyl group in the case that R3 is a hydrogen or a formyl group, and R4 is a hydrogen group or a C1 to C3 haloalkyl group in the case that R3 is a C1 to C3 alkyl group which may be substituted with one or more substituents selected from the following substituent group α.

3-pyrazolyloxypyridazines, herbicidal compositions and uses thereof

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, (2008/06/13)

Disclosed are certain 3-pyrazolyloxypyridazines, compositions thereof which are herbicidal and methods of using such composition for controlling undesired plants. Also disclosed are mixtures of such pyridazines and acetanilide herbicides, to which mixture a safener may be added, if desired. Intermediate compounds useful in preparing the pyrazolyloxypyridazines are also disclosed.

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