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925006-96-8

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925006-96-8 Usage

Uses

Ethyl 5-(4-methoxyphenyl)-isoxazole-3-carboxylate

Check Digit Verification of cas no

The CAS Registry Mumber 925006-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,0,0 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 925006-96:
(8*9)+(7*2)+(6*5)+(5*0)+(4*0)+(3*6)+(2*9)+(1*6)=158
158 % 10 = 8
So 925006-96-8 is a valid CAS Registry Number.

925006-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-(4-methoxyphenyl)-1,2-oxazole-3-carboxylate

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:925006-96-8 SDS

925006-96-8Relevant articles and documents

Synthesis, in vitro anticancer activity and in silico studies of certain isoxazole-based carboxamides, ureates, and hydrazones as potential inhibitors of VEGFR2

Abou-Seri, Sahar M.,Behery, Mohamed G. M.,Eissa, Amal A. M.,Omar, Farghaly A.

, (2021/09/20)

The ensuing research presents the results of in vitro anticancer activity of novel 28 compounds of isoxazole–based carboxamides 3(a-d); ureates 4(a-g), 5, 6, 7a,b, 8; and hydrazones 9(a-f), 10(a-d), 11a,b as potential inhibitors of VEGFR2. The carboxamide

Synthesis of isoxazoles via cyclization of β-fluoro enones with sodium azide

Li, Liangkui,Huang, Shiqing,Mao, Kuantao,Lv, Leiyang,Li, Zhiping

, (2021/04/22)

A practical method for the synthesis of 3,5-disubstituted isoxazoles via cyclization of β-fluoro enones with sodium azide was disclosed. Density functional theory (DFT) calculation indicated that both (1) the azirine formation followed by intramolecular rearrangement and (2) direct enolate O-attack via 5-exo-trig cyclization of vinyl azide were possible for the isoxazole formation.

Development of a continuous flow photoisomerization reaction converting isoxazoles into diverse oxazole products

Bracken, Cormac,Baumann, Marcus

, p. 2607 - 2617 (2020/03/11)

A continuous flow process is presented, which directly converts isoxazoles into their oxazole counterparts via a photochemical transposition reaction. This results in the first reported exploitation of this transformation to establish its scope and synthe

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