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5-isopropyl-1,3-oxazole-4-carboxylic acid(SALTDATA: FREE) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89006-96-2

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89006-96-2 Usage

General Description

5-isopropyl-1,3-oxazole-4-carboxylic acid, also known as SALTDATA: FREE, is a chemical compound with a molecular formula C8H11NO3. It is a derivative of oxazole and carboxylic acid, and is characterized by its isopropyl group. 5-isopropyl-1,3-oxazole-4-carboxylic acid(SALTDATA: FREE) is commonly used in organic synthesis and pharmaceutical research, and may have potential applications in the development of new drugs or medicines. Its properties and potential uses make it an important compound in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 89006-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,0 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89006-96:
(7*8)+(6*9)+(5*0)+(4*0)+(3*6)+(2*9)+(1*6)=152
152 % 10 = 2
So 89006-96-2 is a valid CAS Registry Number.

89006-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-propan-2-yl-1,3-oxazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-(1-methylethyl)-1,3-oxazole-4-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:89006-96-2 SDS

89006-96-2Relevant academic research and scientific papers

Widely Exploited, Yet Unreported: Regiocontrolled Synthesis and the Suzuki–Miyaura Reactions of Bromooxazole Building Blocks

Solomin, Vitalii V.,Radchenko, Dmytro S.,Slobodyanyuk, Evgeniy Y.,Geraschenko, Oleksandr V.,Vashchenko, Bohdan V.,Grygorenko, Oleksandr O.

, p. 2884 - 2898 (2019/03/07)

An approach to synthesis of 2-, 4-, and 5-bromooxazoles is described. The method was optimized, and its scope was extended to all three isomeric parents, as well as various alkyl- and aryl-substituted bromooxazoles. It was found that direct regiocontrolled lithiation followed by reaction with electrophilic bromine source was common for all substrates and led exclusively to the target substituted 2-, 4- and 5-bromooxazoles on multigram scale. The utility of the multipurpose building blocks obtained in this work was demonstrated in the Suzuki–Miyaura cross-coupling reaction under parallel synthesis conditions.

BENZPYRAZOL DERIVATIVES AS INHIBITORS OF PI3 KINASES

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Page/Page column 122-123, (2009/12/28)

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.

NOVEL PHARMACEUTICALS

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Page/Page column 57, (2010/11/28)

The present invention relates to immune response modifiers of formula (I), which act selectively through agonism, of Toll-Like Receptors (TLRs), uses thereof, processes for the preparation thereof, intermediates used in the preparation thereof and compositions containing said inhibitors. These inhibitors have utility in a variety of therapeutic areas including the treatment of infectious disease such as Hepatitis (e.g. HCV, HBV), genetically related viral infection and cancer.

Alkyloxazolylacetic acid derivative for the treatment of hyperlipidemia

-

, (2008/06/13)

A alkyloxazolylacetic acid derivative of the formula: STR1 wherein Ring A is phenyl or halogenophenyl, R1 is lower alkyl of one to 5 carbon atoms and R2 is hydrogen or lower alkyl of one to 3 carbon atoms. The compound (I) is useful

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