79828-16-3

Usage

Type of compound

Pteridine derivative

Aromatic heterocyclic compound

Yes

Structure

Contains a dodecyl (12-carbon) side chain attached to the pteridine ring

Biological activities

Wide range, depending on specific application

Potential uses

Pharmaceutical or research compound

Unique structure

Contributes to its potential biological activities and applications

Solubility

Not specified, but may vary depending on the solvent used

Stability

Not specified, but may be influenced by factors such as temperature, light, and humidity

Reactivity

Not specified, but may react with certain chemicals or under specific conditions

Toxicity

Not specified, but should be handled with care and proper safety measures due to its potential biological activities

Purity

Not specified, but high purity may be required for certain applications, such as pharmaceuticals or research

Storage

Should be stored in a cool, dry, and dark place, away from direct sunlight and moisture

Safety precautions

Use appropriate personal protective equipment (PPE) and follow proper handling procedures to minimize exposure and potential hazards

Regulatory status

Not specified, but may be subject to specific regulations depending on its intended use and application in different countries or regions

Upstream product

• 61066-33-9 pyrimidine-2,4,5,6(1H,3H)-tetraone 
• 64241-76-5 N-1-dodecyl ortho-phenylenediamine 
• 2244-11-3 alloxan monohydrate 
• 95-54-5 1,2-diamino-benzene 
• 112-52-7 1-chlorododecane 
• 3237-50-1 5,5-dihydroxy-pyrimidine-2,4,6-trione 
• 143-15-7 1-dodecylbromide 

Relevant academic research and scientific papers

Supramolecular Chemistry-Based One-Pot High-Efficiency Separation of Solubilizer-Free Pure Semiconducting Single-Walled Carbon Nanotubes: Molecular Strategy and Mechanism

Single-walled carbon nanotubes (SWCNTs) have the potential to revolutionize nanoscale electronics and power sources; however, their low purity and high separation cost limit their use in practical applications. Here we present a supramolecular chemistry-based one-pot, less expensive, scalable, and highly efficient separation of a solubilizer/adsorbent-free pure semiconducting SWCNT (sc-SWCNT) using flavin/isoalloxazine analogues with different substituents. On the basis of both experimental and computational simulations (DFT study), we have revealed the molecular requirements of the solubilizers as well as provided a possible mechanism for such a highly efficient selective sc-SWCNT separation. The present sorting method is very simple (one-pot) and gives a promising sc-SWCNT separation methodology. Thus, the study provides insight for the molecular design of an sc-SWCNT solubilizer with a high (n,m)-chiral selectivity, which benefits many areas including semiconducting nanoelectronics, thermoelectric, bio and energy materials, and devices using solubilizer-free very pure sc-SWCNTs.

Microwave-assisted synthesis of 10-substituted isoalloxazines in the presence of solid acids

The microwave-enhanced synthesis of 10-substituted isoalloxazines is achieved rapidly (～4 min) and in good yield (>80-95%) via the cyclocondensation of 2-substituted aminoanilines with alloxan or N-methylalloxan monohydrate in the presence of acidic alumi

COENZYME MODELS. PART 29. ON THE UNUSUAL SPECTROSCOPIC BEHAVIOUR OF 10-DODECYL-3-METHYLISOALLOXAZINE (AMPHIPHILIC FLAVIN ANALOGUE) IN AQUEOUS SOLUTION.

At room temperature in aqueous solution, the visible absorption peak (S1) of the title isoalloxazine (3) gave a well resolved, three-band fine structure which is believed to appear only in apolar solvents or in enzymatic hydrophobic pockets where isoallox

OXIDATIVE TRAPPING OF TRANSIENT THIAZOLIUM-ALDEHYDE ADDUCTS BY INTRAMOLECULAR FLAVIN. FLAVIN-THIAMINE BISCOENZYME MODEL

A biscoenzime which has within a molecular structure both flavin and thiazolium ion was synthesized.In the presence of the biscoenzyme and hexadecyltrimethylammonium bromide (CTAB) micelle, aldehydes were efficiently converted to carboxylic acids and the acyloin condensation products were scarcely detected. Thus, the biscoenzyme serves as an interesting model system for pyruvate dehydrogenase.