Welcome to LookChem.com Sign In|Join Free
  • or
2,4(1H,3H)-Pyrimidinedione, 1-pentyl-, also known as a synthetic cannabinoid, is a chemical compound characterized by a pyrimidinedione core with a pentyl group attached to the nitrogen atom at the 1 position. It mimics the effects of THC, the active ingredient in marijuana, by interacting with the same receptors in the brain, leading to psychoactive effects. 2,4(1H,3H)-Pyrimidinedione, 1-pentylis often found in products labeled as "herbal incense" or "potpourri" and is considered a designer drug due to its recreational use for marijuana-like effects.

13350-87-3

Post Buying Request

13350-87-3 Suppliers

Recommended suppliers

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

13350-87-3 Usage

Uses

Used in Recreational Drug Use:
2,4(1H,3H)-Pyrimidinedione, 1-pentylis used as a psychoactive substance for its marijuana-like effects, often sought after for recreational purposes. However, its use can have serious health consequences, including seizures, hallucinations, and even fatalities.
Used in Research and Development:
In some cases, 2,4(1H,3H)-Pyrimidinedione, 1-pentylmay be utilized in scientific research to study the effects and mechanisms of action of synthetic cannabinoids on the human brain and body. This can contribute to a better understanding of the risks and potential therapeutic applications associated with these compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 13350-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,5 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13350-87:
(7*1)+(6*3)+(5*3)+(4*5)+(3*0)+(2*8)+(1*7)=83
83 % 10 = 3
So 13350-87-3 is a valid CAS Registry Number.

13350-87-3Downstream Products

13350-87-3Relevant academic research and scientific papers

Copper-Catalyzed Regioselective Direct C–H Thiolation and Thiocyanation of Uracils

Noikham, Medena,Yotphan, Sirilata

, p. 2759 - 2766 (2019)

A novel copper-catalyzed direct C–H thiolation and thiocyanation of uracils using disulfides and thiocyanate salts respectively as coupling partners are described. These reactions enable the C–H bond cleavage and C–S bond formation to proceed efficiently under relatively mild conditions, providing useful methods for a preparation of a series of thio-substituted at the C5 position of uracil derivatives. These protocols exhibit several merits including simple experimental procedures, readily accessible substrates and reagents, broad scopes, high yields, and excellent regioselectivity. Preliminary mechanistic studies revealed that a radical pathway is likely to be involved.

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 13350-87-3