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5-Isopropylisoxazole-3-carboxylic acid is a chemical compound with the molecular formula C8H11NO3, belonging to the class of isoxazole carboxylic acids. It is characterized by its potential anti-inflammatory and analgesic properties and is recognized for its role in the synthesis of pharmaceuticals and agrochemicals. 5-Isopropylisoxazole-3-carboxylic acid is significant in medicinal and organic chemistry due to its potential therapeutic applications and can be synthesized through various chemical processes.

89776-74-9

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89776-74-9 Usage

Uses

Used in Pharmaceutical Industry:
5-Isopropylisoxazole-3-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its potential therapeutic applications. Its anti-inflammatory and analgesic properties make it a valuable component in the development of medications aimed at treating pain and inflammation.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Isopropylisoxazole-3-carboxylic acid is utilized as a building block in the creation of agrochemicals, contributing to the development of products that can enhance crop protection and improve agricultural yields.
Used in Medicinal Chemistry Research:
5-Isopropylisoxazole-3-carboxylic acid serves as a subject of study in medicinal chemistry, where its properties and potential uses in treating various medical conditions are explored. Researchers investigate its mechanisms of action and interactions with biological targets to advance the understanding of its therapeutic potential.
Used in Organic Chemistry:
As a member of the isoxazole carboxylic acids, 5-Isopropylisoxazole-3-carboxylic acid is also important in organic chemistry for its role in the synthesis of complex organic molecules and the exploration of novel chemical reactions and pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 89776-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,7 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89776-74:
(7*8)+(6*9)+(5*7)+(4*7)+(3*6)+(2*7)+(1*4)=209
209 % 10 = 9
So 89776-74-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO3/c1-4(2)6-3-5(7(9)10)8-11-6/h3-4H,1-2H3,(H,9,10)

89776-74-9 Well-known Company Product Price

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  • Aldrich

  • (644730)  5-Isopropylisoxazole-3-carboxylicacid  97%

  • 89776-74-9

  • 644730-1G

  • 1,769.04CNY

  • Detail

89776-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Isopropylisoxazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-propan-2-yl-1,2-oxazole-3-carboxylic acid

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:89776-74-9 SDS

89776-74-9Upstream product

89776-74-9Downstream Products

89776-74-9Relevant academic research and scientific papers

Substituted 1,2,4-triazolo[3,4-a]phthalazine derivatives as GABA alpha 5 ligands

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, (2008/06/13)

Substituted 1,2,4-Triazolo[3,4-A]phthalazine derivatives are GABA Alpha 5 ligands and are represented by the formula

Isoxazole derivatives

-

, (2008/06/13)

Isoxazole derivatives represented by the formula: STR1 are prepared; wherein R1 and R2 each is hydrogen atom, alkyl group of 1 to 8 carbon atoms, or cycloalkyl group of 3 to 10 carbon atoms; R3 and R4 each is hydrogen atom, alkyl group of 1 to 8 carbon atoms, cycloalkyl group of 3 to 10 carbon atoms, or phenyl group; or the group Is morpholino group; and Y is oxo group, thioxo group or imino group; being useful as a hypoglycemic and/or a blood free-fatty-acid normalizing antidiabetic agent.

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