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6-BROMO-4-METHYL-1-PHENYLANTHRAPYRIDONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67499-52-9

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67499-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67499-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,9 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67499-52:
(7*6)+(6*7)+(5*4)+(4*9)+(3*9)+(2*5)+(1*2)=179
179 % 10 = 9
So 67499-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H14BrNO2/c1-12-11-16(24)19-20-18(14-9-5-6-10-15(14)22(19)26)17(23(27)25-21(12)20)13-7-3-2-4-8-13/h2-11H,1H3,(H,25,27)

67499-52-9 Well-known Company Product Price

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  • Aldrich

  • (257273)  6-Bromo-4-methyl-1-phenylanthrapyridone  98%

  • 67499-52-9

  • 257273-100G

  • 586.17CNY

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67499-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Bromo-4-methyl-1-phenylanthrapyridone

1.2 Other means of identification

Product number -
Other names 1-Phenyl-6-bromo-4-methyl-3H-dibenz(f,ij)isoquinoline-2,7-dione

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:67499-52-9 SDS

67499-52-9Downstream Products

67499-52-9Relevant academic research and scientific papers

Synthesis and color properties of novel polymeric dyes based on grafting of anthraquinone derivatives onto O-carboxymethyl chitosan

Lv, Dongjun,Cui, Jin,Wang, Yufang,Zhu, Guohua,Zhang, Mingjie,Li, Xiujing

, p. 33494 - 33501 (2017/07/13)

Four polymeric dyes were prepared by grafting brominated anthraquinone derivatives onto O-carboxymethyl chitosan through Ullmann condensation. The chemical structure of the prepared polymeric dyes was determined by Fourier transform infrared spectroscopy (FT-IR), elemental analysis and differential scanning calorimetry (DSC), and the results showed that the anthraquinone derivatives were successfully grafted onto O-carboxymethyl chitosan. The grafting degrees of the four polymeric dyes were 0.66, 1.14, 0.93 and 1.01 mmol g-1 respectively. The color performance of brominated anthraquinone derivatives and prepared polymeric dyes was determined and compared using digital photographs and UV-Vis adsorption spectra, and it was found that the electronic properties and planarity of the substituent group in the anthraquinone derivatives obviously affected the adsorption wavelength of the prepared polymeric dyes. In addition, the polymeric dyes with an electron donating group and higher planarity showed longer adsorption wavelengths and more deep color. The cytotoxicity of prepared polymeric dyes was tested, and their IC50 values on human liver cell lines LO2 were 7.666, 8.557, 8.186 and 8.934 g L-1 respectively, suggesting low cytotoxicity of the prepared polymeric dyes.

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