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392-08-5

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392-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 392-08-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 392-08:
(5*3)+(4*9)+(3*2)+(2*0)+(1*8)=65
65 % 10 = 5
So 392-08-5 is a valid CAS Registry Number.

392-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-fluoro-2-hydroxyphenyl)-3-(4-methoxyphenyl)propenone

1.2 Other means of identification

Product number -
Other names 4'-Fluor-4-methoxy-2'-hydroxy-chalkon

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:392-08-5 SDS

392-08-5Relevant articles and documents

Synthesis, characterization and biological evaluation of novel 4′-fluoro-2′-hydroxy-chalcone derivatives as antioxidant, anti-inflammatory and analgesic agents

Abdellatif, Khaled R. A.,Elshemy, Heba A. H.,Salama, Samir A.,Omar, Hany A.

, p. 484 - 491 (2015)

In an effort to develop safe and potent anti-inflammatory agents, a series of novel 4′-fluoro-2′-hydroxychalcones 5a-d and their dihydropyrazole derivatives 6a-d was prepared. It was synthesized via aldol condensation of 4′-fluoro-2′-hydroxyacetophenone w

Pyrrolidylsubstituted azadipyrromethene with fully chelated boron atom

Yakubovskyi, Viktor P.,Shandura, Mykola P.,Kovtun, Yuriy P.

scheme or table, p. 944 - 950 (2010/06/12)

A difluorosubstituted aza-boron-dipyrromethene derivative with fully chelated boron atom was synthesized by the reaction of BF3Et 2O with 3,3,5,5-tetraarylazadipyrromethene, which was easily prepared from 1,3-diaryl-4-nitro-butan-1-one and ammonium acetate. One fluorine atom of the dye was substituted by pyrrolidine residue. This resulted in a significant bathochromic effect. Ultraviolet absorption and fluorescence emission spectra were recorded, and quantum yields of the obtained compounds were calculated.

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