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4-(3,5-dimethoxybenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one is a complex organic compound with the molecular formula C18H15NO4. It is characterized by a 1,3-oxazol-5(4H)-one core structure, which features a five-membered ring with an oxygen atom and a nitrogen atom. The compound has a phenyl group attached to the 2-position of the oxazolone ring and a 3,5-dimethoxybenzylidene group at the 4-position. The dimethoxybenzylidene moiety consists of a benzene ring with two methoxy groups at the 3 and 5 positions, and a carbonyl group (C=O) that forms a double bond with the oxazolone ring. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity.

1097-21-8

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1097-21-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1097-21-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1097-21:
(6*1)+(5*0)+(4*9)+(3*7)+(2*2)+(1*1)=68
68 % 10 = 8
So 1097-21-8 is a valid CAS Registry Number.

1097-21-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(3,5-dimethoxyphenyl)methylidene]-2-phenyl-1,3-oxazol-5-one

1.2 Other means of identification

Product number -
Other names 5-Oxo-2-phenyl-4-(3,5-dimethoxy-phenyl)-4,5-dihydro-oxazol

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:1097-21-8 SDS

1097-21-8Relevant academic research and scientific papers

Synthesis and neurotoxic potential of racemic and chiral dihydroxytetrahydroquinoline derivatives

Lewis, Russell J.,Francis, Charles A.,Lehr, Roland E.,Leroy Blank

, p. 5345 - 5352 (2007/10/03)

The synthesis and preliminary neurotoxic investigation of (±), (+) and (-)-3-amino-6,7-dihydroxy-1,2,3,4-tetrahydroquinoline, (±)-3-amino-6,8-dihydroxy-1,2,3,4-tetrahydroquinoline and (±)-3-aminomethyl-6,7-dihydroxy-1,2,3,4-tetrahydroquinoline are described. While exhibiting relatively no dopamine and only moderate norepinephrine depletions, these compounds elicit serotonin depletions equal to those provided by the well-known serotonergic neurotoxin 5,7-dihydroxytryptamine in whole mouse brain. (C) 2000 Elsevier Science Ltd.

Combretastatin Analogs via Hydration of Stilbene Derivatives

Mannila, Erkki,Talvitie, Antti

, p. 1037 - 1040 (2007/10/02)

Hydration of the double bond of some stilbene congeners of Picea abies bark by TiCl4.NaBH4 reagent is described.Five racemic 1,2-diphenylethanol derivatives (9-13), structurally related to (R)-(-)combretastatin , have been obtained and characterize

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