157401-06-4

Basic information

• Product Name: 2,4(1H,3H)-Pyrimidinedione, 1-[3-(2-furanyl)-2-propenyl]-5-methyl-6-(phenylthio)-, (E)-
• CAS NO: 157401-06-4
• Molecular Formula: C18H16N2O3S
• Molecular Weight: 340.403
• Mol File: 157401-06-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,4(1H,3H)-Pyrimidinedione, 1-[3-(2-furanyl)-2-propenyl]-5-methyl-6-(phenylthio)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4(1H,3H)-Pyrimidinedione, 1-[3-(2-furanyl)-2-propenyl]-5-methyl-6-(phenylthio)-, (E)-(157401-06-4)
• EPA Substance Registry System: 2,4(1H,3H)-Pyrimidinedione, 1-[3-(2-furanyl)-2-propenyl]-5-methyl-6-(phenylthio)-, (E)-(157401-06-4)

Safety Data

• Hazardous Substances Data: 157401-06-4(Hazardous Substances Data)

Usage

Core structure

The compound has a pyrimidinedione core structure, which is a six-membered ring with two oxygen atoms in the 2 and 4 positions.

Substituents

The core structure is substituted with a furanyl group (a five-membered ring with a carbonyl group), a propenyl group (a three-carbon chain with a double bond and a methyl group), a methyl group, and a phenylthio group (a phenyl ring with a sulfur atom).

Configuration

The compound exists in the E configuration, indicating the specific arrangement of the double bond in the propenyl group.

Industrial applications

The compound may have various industrial applications, such as in pharmaceuticals, agrochemicals, or materials science, based on its structural features and potential reactivity.

Properties and potential hazards

More detailed information is required for a comprehensive understanding of the compound's properties, uses, and potential hazards.

Upstream product

• 539-47-9 3-(fur-2-yl)crotonic acid 
• 189637-50-1 C₁₀H₁₀O₅ 
• 136160-18-4 5-methyl-6-(phenylthio)pyrimidine-2,4(1H,3H)-dione 
• 132774-43-7 1-<(benzyloxy)methyl>-6-(phenylthio)thymine 
• 27393-97-1 (E)-3-(2-furanyl)-2-propen-1-ol 
• 118813-17-5 (E)-2-(3-acetoxyprop-1-enyl)furan 

Relevant articles and documents

Synthesis and anti-HIV activity of novel N-1 side chain-modified analogs of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT)

A series of 33 N-1 side chain-modified analogs of 1-[(2- hydroxyethoxy)methyl]-6-(phenylthio)thymine (1, HEPT) were synthesized and evaluated for their anti-HIV-1 activity. In particular, the influence of substitution of the terminal hydroxy group of the acyclic structure of HEPT and the structural rigidity of this side chain were investigated. Halo (7, 8), azido (9), and amino (10-15) derivatives were synthesized from HEPT via the p-tosylate derivative 6. Acylation of the primary amine 15 afforded the amido analogs 16-20. The diaryl derivatives 26-29 were prepared by reaction of HEPT, or of the 6-(2-pyridylthio) analog 23, with diaryl disulfides in the presence of tri-n-butylphosphine. Compounds 39-41, in which the N-1 side chain is rigidified by incorporation of an E-configured double bond, were obtained by palladium(0)-catalyzed coupling of several different 6- (arylthio)uracil derivatives (37, 38) with allyl acetates 33. Compounds 13, 40a,c,d,f, and 41, incorporating an aromatic ring at the end of the acyclic side chain, were found to be more potent than the known diphenyl-substituted HEPT analog BPT (2), two of them, 40c,d, being 10-fold more active.