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1128-71-8

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1128-71-8 Usage

General Description

4-(1,3-oxazol-5-yl)phenol is a chemical compound with the molecular formula C10H7NO2. It is a phenolic compound that contains an oxazole ring and a hydroxyl group. This chemical is typically used in organic synthesis and medicinal chemistry. It has been studied for its potential biological activities, including its antioxidant and antimicrobial properties. The compound has also been investigated for its potential use in the development of new pharmaceuticals and agrochemicals. Additionally, it may have potential applications in the field of materials science and nanotechnology. Overall, 4-(1,3-oxazol-5-yl)phenol is a versatile compound with a range of potential uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1128-71-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1128-71:
(6*1)+(5*1)+(4*2)+(3*8)+(2*7)+(1*1)=58
58 % 10 = 8
So 1128-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO2/c11-8-3-1-7(2-4-8)9-5-10-6-12-9/h1-6,11H

1128-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-Oxazolyl)phenol

1.2 Other means of identification

Product number -
Other names 4-(1,3-oxazol-5-yl)phenol

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:1128-71-8 SDS

1128-71-8Relevant articles and documents

Structure-Activity Relationships of New Natural Product-Based Diaryloxazoles with Selective Activity against Androgen Receptor-Positive Breast Cancer Cells

Robles, Andrew J.,McCowen, Shelby,Cai, Shengxin,Glassman, Michaels,Ruiz, Francisco,Cichewicz, Robert H.,McHardy, Stanton F.,Mooberry, Susan L.

, p. 9275 - 9289 (2017/11/30)

Targeted therapies for ER+/PR+ and HER2-amplified breast cancers have improved patient survival, but there are no therapies for triple negative breast cancers (TNBC) that lack expression of estrogen and progesterone receptors (ER/PR), or amplification or

Mild palladium-catalyzed regioselective direct arylation of azoles promoted by tetrabutylammonium acetate

Bellina, Fabio,Lessi, Marco,Manzini, Chiara

, p. 5621 - 5630 (2013/09/12)

A mild, general, and convenient palladium-catalyzed direct arylation of the 5-position of azoles with aryl bromides, efficiently promoted by tetrabutylammonium acetate, is described. 1-Methylpyrazole, oxazole, and thiazole reacted at 70°C in N,N-dimethyla

CCR5 ANTAGONISTS AS THERAPEUTIC AGENTS

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Page/Page column 27, (2009/07/17)

The present invention relates to compounds useful in the treatment of CCR5-related diseases and disorders, for example, useful in the inhibition of HIV replication, the prevention or treatment of an HIV infection, and in the treatment of the resulting acq

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