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3-ISOPROPYLISOXAZOLE-5-CARBOXYLIC ACID is a chemical compound with the molecular formula C7H9NO3. It is an isoxazole derivative with a carboxylic acid functional group at the 5-position and an isopropyl group at the 3-position. 3-ISOPROPYLISOXAZOLE-5-CARBOXYLIC ACID is known for its antimicrobial and pesticidal properties, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Its structural features and biological activities also contribute to its potential applications in medicinal chemistry and drug discovery.

14633-22-8

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14633-22-8 Usage

Uses

Used in Pharmaceutical Industry:
3-ISOPROPYLISOXAZOLE-5-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various biologically active molecules, including pharmaceuticals. Its antimicrobial and pesticidal properties make it a valuable component in the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical industry, 3-ISOPROPYLISOXAZOLE-5-CARBOXYLIC ACID is used as a building block for the synthesis of agrochemicals. Its antimicrobial and pesticidal properties contribute to the development of effective products for crop protection and pest control.
Used in Medicinal Chemistry and Drug Discovery:
3-ISOPROPYLISOXAZOLE-5-CARBOXYLIC ACID is utilized as a structural component in medicinal chemistry and drug discovery. Its unique features and biological activities make it a promising candidate for the development of novel therapeutic agents and pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 14633-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,3 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14633-22:
(7*1)+(6*4)+(5*6)+(4*3)+(3*3)+(2*2)+(1*2)=88
88 % 10 = 8
So 14633-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO3/c1-4(2)5-3-6(7(9)10)11-8-5/h3-4H,1-2H3,(H,9,10)

14633-22-8SDS

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 3-propan-2-yl-1,2-oxazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Isopropyl-5-carboxy-isoxazol

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:14633-22-8 SDS

14633-22-8Relevant academic research and scientific papers

Structural hybridization of pyrrolidine-based T-type calcium channel inhibitors and exploration of their analgesic effects in a neuropathic pain model

Son, Woo Seung,Jeong, Kyu-Sung,Lim, Sang Min,Pae, Ae Nim

, p. 1168 - 1172 (2019)

Highly effective and safe drugs for the treatment of neuropathic pain are urgently required and it was shown that blocking T-type calcium channels can be a promising strategy for drug development for neuropathic pain. We have developed pyrrolidine-based T

Novel pyrrolidine or piperidine derivatives having activity for T-type calcium channel

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Paragraph 0218-0221, (2020/04/23)

A pyrrolidine or piperidine compound having activity for T - type calcium channel, wherein the pyrrolidine or piperidine compound of Formula 1 according to the present invention has an excellent antagonistic activity to, T-type calcium channel, and can be used as a preventive or therapeutic agent, for pain diseases, or cancer related to cancer, or cancer such as, epilepsy and,hepatic pain, angina. (by machine translation)

Ramoplanin derivatives possessing antibacterial activity

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Page/Page column 39; 50, (2010/11/23)

Novel ramoplanin derivatives are disclosed. These ramoplanin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against gram positive bacteria, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.

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