Welcome to LookChem.com Sign In|Join Free
  • or
5,5'-Dichloroatranorin is a synthetic chemical compound with the molecular formula C14H8Cl2O2. It is a derivative of atranol, a naturally occurring compound found in the roots of the plant Atropa belladonna, commonly known as deadly nightshade. 5,5'-Dichloroatranorin is characterized by the presence of two chlorine atoms attached to the central benzene ring, which distinguishes it from other atranol derivatives. 5,5'-dichloroatranorin is primarily used in the pharmaceutical industry for its anti-inflammatory and analgesic properties, similar to its parent compound atranol. It is also known for its potential applications in the treatment of various inflammatory conditions and pain management. However, due to its synthetic nature and potential side effects, 5,5'-dichloroatranorin is not as widely used as some other derivatives and requires further research to fully understand its safety and efficacy.

984-95-2

Post Buying Request

984-95-2 Suppliers

Recommended suppliers

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

984-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 984-95-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,8 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 984-95:
(5*9)+(4*8)+(3*4)+(2*9)+(1*5)=112
112 % 10 = 2
So 984-95-2 is a valid CAS Registry Number.

984-95-2Upstream product

984-95-2Relevant academic research and scientific papers

Chemical constituents of the lichen, Candelaria concolor: A complete NMR and chemical degradative investigation

Dias, Daniel A.,Urban, Sylvia

, p. 925 - 939 (2009)

A detailed chemical and spectroscopic investigation of the terrestrial lichen Candelaria concolor has yielded several lichenic metabolites belonging to the pulvinic acid series, as well as several depside derivatives including pulvinic dilactone (1), vulpinic acid (4) and calycin (5). The chemical transformation of 1 to pulvinic acid (3) is reported for the first time, as is the conversion of atranorin (6) to 5-chloroatranorin (7) and then finally to 5,5'-dichloroatranorin (8) under very mild conditions. Also presented is the complete 1D and 2D NMR assignment for compounds 1, 3, 4, 5 and 8, including partial NMR chemical shift assignments for the unstable depside (7). Previously, these metabolites had only been partially assigned by NMR spectroscopy.

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 984-95-2