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2H-1-Benzopyran-2-one, 3-[5-(4-hydroxy-3-methoxyphenyl)-1,3,4-oxadiazol-2-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143814-60-2

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143814-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143814-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,8,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 143814-60:
(8*1)+(7*4)+(6*3)+(5*8)+(4*1)+(3*4)+(2*6)+(1*0)=122
122 % 10 = 2
So 143814-60-2 is a valid CAS Registry Number.

143814-60-2SDS

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 3-[5-(4-Hydroxy-3-methoxy-phenyl)-[1,3,4]oxadiazol-2-yl]-chromen-2-one

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:143814-60-2 SDS

143814-60-2Downstream Products

143814-60-2Relevant academic research and scientific papers

Synthesis of 3-(5-phenyl-1, 3,4-oxadiazol-2-yl)-2H-chromen-2-ones as anticonvulsant agents

Naga Sudha,Girija Sastry,Sai Harika,Yellasubbaiah

, p. 737 - 745 (2019/05/22)

3-(5-Phenyl-l,3,4-oxadiazol-2-yl)-2H-chromen-2-one (IVa-IVl) have been synthesized from N-benzylidene2-oxo-2#- chromene-3-carbohydrazide (IIIa-IIIl). The structure of synthesized coumarinyl oxadiazoles have been established by spectral data, elemental ana

Coumarin congeners as antidepressants

Singh,Srivastava,Palit,Shanker

, p. 993 - 996 (2007/10/02)

3-Carboethyl coumarin (I) was converted to coumarin 3-acid hydrazide (II). This on reaction with appropriate aldehyde yielded 3-arylidino amino coumarin (III). Compound III on diazotisation and reaction with ferric chloride yielded the corresponding formazans viz. 3-substituted phenyl azoarylidino, amido coumarins (IVa1-a10) and oxadiazoles viz. 2-aryl-5-(3-coumarinyl)-1,3,4-oxadiazoles (Va1-a3), respectively. Simultaneously 3-carboethyl coumarin on hydrolysis gave 3-carboxy coumarin (VI) which on reaction with aryl amine in methylene chloride yielded 3-(N-aryl)amido coumarin (VIIa1-a3). The compounds were screened for their antidepressant activity against a tricyclic antidepressant (imipramine). Compounds IVa4, IVa5 and IVa9 exhibited activity better than imipramine with no toxicity (ALD50 > 1000 mg/kg) but IVa5 showed some side effects.

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