141178-50-9 Usage
Ester derivative
pyrazole-3-carboxylic acid The compound is derived from pyrazole-3-carboxylic acid, which is a five-membered heterocyclic ring system containing one nitrogen and one carboxyl group.
Common uses
pharmaceuticals, agrochemicals 1H-Pyrazole-3-carboxylic acid, 1,1-dimethylethyl ester (9CI) is commonly used in the production of pharmaceuticals and agrochemicals due to its versatile chemical properties.
Physical properties
colorless liquid, fruity odor The compound is a colorless liquid with a fruity smell, which may be relevant in applications such as flavoring or fragrances.
Solubility
insoluble in water, soluble in organic solvents 1H-Pyrazole-3-carboxylic acid, 1,1-dimethylethyl ester (9CI) does not dissolve in water but dissolves in many organic solvents, which can be important for its use in various chemical reactions and processes.
Industrial applications
solvent, chemical intermediate, reagent in organic synthesis The compound has a variety of industrial applications, including use as a solvent, a chemical intermediate, and a reagent in organic synthesis.
Additional uses
dyes, pigments, new materials 1H-Pyrazole-3-carboxylic acid, 1,1-dimethylethyl ester (9CI) is also used in the manufacturing of dyes and pigments, as well as in the development of new materials, showcasing its versatility in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 141178-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,7 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141178-50:
(8*1)+(7*4)+(6*1)+(5*1)+(4*7)+(3*8)+(2*5)+(1*0)=109
109 % 10 = 9
So 141178-50-9 is a valid CAS Registry Number.
141178-50-9Relevant articles and documents
COMPOUNDS AND USES THEREOF
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Page/Page column 155, (2020/08/22)
The present disclosure features compounds useful for the treatment of BAF complex-related disorders.
Convenient synthesis of vinyldiazomethanes from α-diazo-β-keto esters and related systems
Davies,Hougland,Cantrell Jr.
, p. 971 - 978 (2007/10/02)
A series of vinydiazomethanes were readily prepared by sodium borohydride reduction of α-diazo-β-ketoesters followed by phosphorus oxychloride induced by dehydration of the resulting α-diazo-β-hydroxyesters.
