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4-(oxazol-4-yl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57801-65-7

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57801-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57801-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,0 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57801-65:
(7*5)+(6*7)+(5*8)+(4*0)+(3*1)+(2*6)+(1*5)=137
137 % 10 = 7
So 57801-65-7 is a valid CAS Registry Number.

57801-65-7SDS

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-(1,3-oxazol-4-yl)phenol

1.2 Other means of identification

Product number -
Other names -

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:57801-65-7 SDS

57801-65-7Relevant articles and documents

SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT

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Page/Page column 60, (2009/12/02)

Substituted cyclopropyl compounds of formula (I) are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. Pharmaceutically acceptable salts and solvates are included as well. The compounds are useful as agonists of the g-protein coupled receptor GPR-119.

Discovery of potent and orally bioavailable heterocycle-based β3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Lafontaine, Jennifer A.,Day, Robert F.,Dibrino, Joe,Hadcock, John R.,Hargrove, Diane M.,Linhares, Michael,Martin, Kelly A.,Maurer, Tristan S.,Nardone, Nancy A.,Tess, David A.,DaSilva-Jardine, Paul

, p. 5245 - 5250 (2008/03/13)

A novel series of heterocycle-based analogs were prepared and evaluated for their in vitro and in vivo biological activity as human β3-adrenergic receptor (AR) agonists. Several analogs demonstrated potent agonist activity at the β3-

Method for enhancement of chemiluminescence

-

, (2008/06/13)

A method for enhancing chemiluminescence which uses a heterocyclic compound of the formula: STR1 wherein R1 is an oxygen or sulfur atom or an imino group optionally substituted by 4-hydroxyphenyl, and R2, R3 and R4 are a hydrogen or halogen atom, an optionally substituted hydrocarbon residue, a heterocyclic group or the like in a luminescence system.

Synthesis and analgesic-antiinflammatory activity of some 4- and 5-substituted heteroarylsalicylic acids

Jones,Fordice,Greenwald,Hannah,Jacobs,Ruyle,Walford,Shen

, p. 1100 - 1104 (2007/10/05)

We have made a series of 4- and 5-aryl- and 4- and 5-heteroarylsalicylic acid derivatives with the objective of reducing gastric irritation and increasing potency. Here we describe a series of 4- and 5-heterocyclic salicylic acids and their antiinflammatory-analgesic potencies measured in comparison to aspirin. An improvement of the therapeutic index over aspirin of 100 was achieved; however, the heterocyclic salicylic acids lacked antipyretic activity. Some physicochemical parameters which may bear on the antiinflammatory activity of these compounds are discussed.

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