Welcome to LookChem.com Sign In|Join Free
  • or
6,8-dihydroxy-3-(hydroxymethyl)-1-methoxyanthra-9,10-quinone is a complex organic compound with the molecular formula C16H12O6. It is a derivative of anthraquinone, a type of quinone that is widely found in nature and has various applications in the pharmaceutical, dye, and chemical industries. This specific compound features two hydroxyl groups at the 6 and 8 positions, a hydroxymethyl group at the 3 position, and a methoxy group at the 1 position. Its structure and properties make it a potential candidate for various chemical reactions and applications, such as in the synthesis of pharmaceuticals or as a precursor for the production of dyes. The compound's unique functional groups also make it a subject of interest for researchers studying the properties and reactivity of anthraquinone derivatives.

478-35-3

Post Buying Request

478-35-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

478-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478-35-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 478-35:
(5*4)+(4*7)+(3*8)+(2*3)+(1*5)=83
83 % 10 = 3
So 478-35-3 is a valid CAS Registry Number.

478-35-3Downstream Products

478-35-3Relevant academic research and scientific papers

Characterization of emodin metabolites in Raji cells by LC-APCI-MS/MS

Koyama, Junko,Takeuchi, Atsuko,Morita, Izumi,Nishino, Yu,Shimizu, Maki,Inoue, Munetaka,Kobayashi, Norihiro

, p. 7493 - 7499 (2009)

A rapid, simple, and sensitive liquid chromatography-atmospheric pressure chemical ionization tandem mass spectrometry (LC-APCI-MS/MS) method was developed for the identification and quantification of emodin metabolites in Raji cells, using aloe-emodin as an internal standard. Analyses were performed on an LC system employing a Cosmosil 5C18 AR-II column and a stepwise gradient elution with methanol-20 mM ammonium formate at a flow rate of 1.0 mL/min operating in the negative ion mode. As a result, the starting material emodin and its five metabolites were detected by analyzing extracts of Raji cells that had been cultivated in the presence of emodin. The identification of the metabolites and elucidation of their structures were performed by comparing their retention times and spectral patterns with those of synthetic samples. In addition to the major metabolite 8-O-methylemodin, four other metabolites were assigned as ω-hydroxyemodin, 3-O-methyl-ω-hydroxyemodin, 3-O-methylemodin (physcion), and chrysophanol.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 478-35-3