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4-OXO-4-PYRIDIN-4-YL-BUTYRIC ACID ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25370-46-1

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25370-46-1 Usage

Uses

γ-Pyridyl- and γ-quinolylbutyrolactones as potential anthelmintics.

Check Digit Verification of cas no

The CAS Registry Mumber 25370-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,7 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25370-46:
(7*2)+(6*5)+(5*3)+(4*7)+(3*0)+(2*4)+(1*6)=101
101 % 10 = 1
So 25370-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO3/c1-2-15-11(14)4-3-10(13)9-5-7-12-8-6-9/h5-8H,2-4H2,1H3

25370-46-1Relevant academic research and scientific papers

NEW COMPOUNDS FOR TREATMENT OF DISEASES RELATED TO DUX4 EXPRESSION

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Page/Page column 58; 89, (2021/06/04)

The present invention relates to compounds for the treatment of diseases related to DUX4 expression, such as muscular dystrophies. It also relates to use of such compounds, or to methods of use of such compounds.

1-butyl-3-methylimidazolium bromide as a solvent and precatalyst for stetter reaction

Phungpis, Baramee,Hahnvajanawong, Viwat

, p. 2028 - 2032 (2020/09/02)

Stetter reaction between aromatic aldehydes and acrylonitrile/ethyl acrylate performing in [Bmim]Br in the presence of NaOH is described. N-Heterocyclic carbene (NHC) generates in situ is shown to be an efficient catalyst. Benzoin condensation also occured as side reaction.

Studies on non-thiazolidinedione antidiabetic Agents. 2. Novel oxyiminoalkanoic acid derivatives as potent glucose and lipid lowering agents

Imoto, Hiroshi,Sugiyama, Yasuo,Kimura, Hiroyuki,Momose, Yu

, p. 138 - 151 (2007/10/03)

We previously reported that (Z)-2-{4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methoxy]benzyloxyimino}-2-(4-phenoxyphenyl)acetic acid (3) showed potent glucose and lipid lowering effects in genetically obese and diabetic mice, KKA y. This compound a

Oxyiminoalkanoic acid derivatives with hypoglycemic and hypolipidemic activity

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, (2008/06/13)

This invention provides a novel oxyiminoalkanoic acid derivative which has excellent hypoglycemic and hypolipidemic actions and which is used for the treatment of diabetes mellitus, hyperlipemia, insulin insensitivity, insulin resistance and impaired glucose tolerance.

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