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5(4H)-Oxazolone, 4-[(2-nitrophenyl)methylene]-2-phenyl-, (4Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66949-10-8

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66949-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66949-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,4 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66949-10:
(7*6)+(6*6)+(5*9)+(4*4)+(3*9)+(2*1)+(1*0)=168
168 % 10 = 8
So 66949-10-8 is a valid CAS Registry Number.

66949-10-8SDS

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 (Z)-4-(2-Nitrobenzylidene)-2-phenyloxazol-5(4H)-one

1.2 Other means of identification

Product number -
Other names 4-((trimethylsilyl)oxy)phenyl magnesium bromide

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:66949-10-8 SDS

66949-10-8Relevant academic research and scientific papers

Synthesis of some novel imidazolinones

Bhatt, Pralav V.,Wadia, Devang N.,Patel, Rajni M.,Patel, Pravin M.

, p. 79 - 82 (2006)

Imidazolinone derivatives of 4a-1 have been prepared by the condensation of known heterocyclic drug derivative with 5-oxazolone derivatives, which were prepared by Erlenmeyer condensation of benzoyl glycine with different aldehydes in the presence of sodium acetate and acetic anhydride. The compounds 3a-1 were further reacted with 5H-dibenzo (b,f) azepine -5-acid hydrazide 2 to give 4a-1 in basic condition. The constitution of the products has been supported by IR, 1H-NMR, Mass spectra and elemental analysis data.

Cyclocondensation reactions of heterocyclic carbonyl compounds XI [1]. Synthesis and study of cyclocondensation reactions of some 3-substituted-5-(2- aminobenzyl)-1H-[1,2,4]triazine-6-ones

Gucky, Tomas,Slouka, Jan,Malon, Michal,Frysova, Iveta

, p. 613 - 621 (2007/10/03)

A series of 2-substituted-4-(2-nitrobenzylidene)-4,5-dihydrooxazol-5-ones (2a-2i) was prepared by the Erlenmeyer's synthesis of 2-nitrobenzaldehyde with acylglycines (1a-1i) and the series of corresponding aminoderivatives (3b-3d and 3g-3i) was synthetise

Calcium acetate catalyzed synthesis of 4-arylidene-2-phenyl-5(4H)- oxazolones under solvent-free conditions

Paul, Satya,Nanda, Puja,Gupta, Rajive,Loupy, André

, p. 425 - 427 (2007/10/03)

Eight 4-arylidene-2-phenyl-5(4H)-oxazolones (azlactones) have been prepared via Erlenmeyer synthesis from aromatic aldehydes and hippuric acid using calcium acetate under solvent-free conditions with microwave irradiation.

Oxazolone analogs as amyloid aggregation inhibitors and for the treatment of alzheimer's disease and disorders related to amyloidosis

-

, (2008/06/13)

Disclosed are compounds of the Formula I and their use in a method of inhibiting the aggregation of amyloid proteins and in a method of imaging amyloid deposits.

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