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4-OXO-2-PHENYL-4H-CHROMENE-6-CARBALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50549-48-9

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50549-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50549-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,4 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50549-48:
(7*5)+(6*0)+(5*5)+(4*4)+(3*9)+(2*4)+(1*8)=119
119 % 10 = 9
So 50549-48-9 is a valid CAS Registry Number.

50549-48-9SDS

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 flavone-6-carboxaldehyde

1.2 Other means of identification

Product number -
Other names 6-flavonecarboxaldehyde

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:50549-48-9 SDS

50549-48-9Relevant academic research and scientific papers

Intervention in cyclophosphamide induced oxidative stress and DNA damage by a flavonyl-thiazolidinedione based organoselenocyanate and evaluation of its efficacy during adjuvant therapy in tumor bearing mice

Roy, Somnath Singha,Chakraborty, Pramita,Bhattacharya, Sudin

, p. 195 - 209 (2014/01/23)

A novel flavonyl-thiazolidinedione based organoselenocyanate compound was synthesized and established as nontoxic at the doses of 2.5 and 5 mg/kg b.w. in mice. Oral administration of the compound in combination with cyclophosphamide (CP) resulted in an im

Synthesis and biological activity of some new flavonyl-2,4-thiazolidinediones

Bozdag-Duendar, Oya,Verspohl, Eugen J.,Das-Evcimen, Net,Kaup, Rebecca M.,Bauer, Katrin,Sarikaya, Mutlu,Evranos, Beguem,Ertan, Rahmiye

, p. 6747 - 6751 (2008/12/23)

A new series of flavonyl-2,4-thiazolidinediones (Va-c, VIa-c) was prepared by Knoevenagel reaction. The synthesized compounds were tested for their ability to inhibit rat kidney aldose reductase (AR) and for their insulinotropic activities in INS-1 cells.

Synthesis and hypoglycemic activity of some new flavone derivatives: 4th communication: 6-flavonyl-2,4-thiazolidinediones

Bozdag-Duendar,Waheed,Verspohl,Ertan

, p. 623 - 627 (2007/10/03)

A new series of flavonyl compounds (1-10) was prepared and tested for their insulinotropic activities in INS-1 cells. Compounds 2, 5 and 6 (at higher concentrations) and compounds 3 and 7-10 were able to increase insulin release in the presence of 5.6 mmo

Unsymmetrical Bichromonyl Benzene Derivatives from Formyl Flavones

Wurm, Gotthard,Nordmann, Matthias

, p. 555 - 558 (2007/10/02)

New flavones (4b-f/6) with formyl functions in the 3-, 4'-, 6- and 4',6-positions are synthesized from bromomethyl or dibromomethyl flavone derivatives (3a-e) with methylflavones (2a-e) as starting compounds.The formyl flavones are suitable synthetic tool

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