2308-61-4

Usage

Uses

Used in Pharmaceutical Industry:
3,6-Dibenzylhexahydropyrazine-2,5-dione is used as an anthelminthic agent for the treatment of parasitic infections. It is effective against various helminths, including intestinal worms and other parasites, providing a new alternative for the treatment of parasitic diseases.
Used in Agricultural Industry:
3,6-Dibenzylhexahydropyrazine-2,5-dione is used as a biopesticide for the control of plant pathogens and pests. Its antibacterial properties make it a promising candidate for the development of eco-friendly and effective biopesticides to protect crops and enhance agricultural productivity.
Used in Cosmetic Industry:
3,6-Dibenzylhexahydropyrazine-2,5-dione is used as an antimicrobial agent in cosmetic products. Its ability to inhibit the growth of bacteria and other microorganisms makes it a valuable ingredient for the development of skincare products, ensuring their safety and efficacy.
Used in Food Industry:
3,6-Dibenzylhexahydropyrazine-2,5-dione is used as a preservative in the food industry. Its antibacterial properties help to extend the shelf life of food products by preventing the growth of spoilage-causing microorganisms, ensuring food safety and quality.

InChI:InChI=1/C18H18N2O2/c21-17-15(11-13-7-3-1-4-8-13)19-18(22)16(20-17)12-14-9-5-2-6-10-14/h1-10,15-16H,11-12H2,(H,19,22)(H,20,21)/t15-,16-/m1/s1

Upstream product

• 150-30-1 Phenylalanine 
• 60-29-7 diethyl ether 
• 64-17-5 ethanol 
• 508220-75-5 2-azidocarbonyl-3-phenyl-propionic acid 
• 2308-61-4 3,6-dibenzylpiperazine-2,5-dione 
• 15028-44-1 DL-phenylalanine methyl ester 
• 126727-04-6 2-(9-fluorenylmethoxycarbonylamino)-3-phenylpropionic acid 
• 100-52-7 benzaldehyde 
• 63-91-2 L-phenylalanine 
• 1233-98-3 3,6-dibenzylidene-2,5-piperazinedione 
• 64-19-7 acetic acid 
• 3182-93-2 (L)-phenylalanine ethyl ester hydrochloride 
• 1795-96-6 phenylalanine ethyl ester 
• 74720-33-5 (Z)-3-(Z)-6-dibenzylidene-2,5-piperazinedione 

Downstream Products

• 103511-63-3 3,6-dibenzyl-1,4-bis-(N,N-phthaloyl-glycyl)-piperazine-2,5-dione 
• 87869-00-9 (3R,6R)-3,6-Dibenzyl-3,6-bis-methylsulfanyl-piperazine-2,5-dione 
• 74156-60-8 3,6-dibenzyl-2,5-dichloropyrazine 
• 132213-60-6 3,6-dibenzyl-5-chloropyrazine 
• 13795-55-6 (+/-)-cis-3,6-dibenzyl-1,4-dimethylpiperazine-2,5-dione 
• 61139-44-4 cyclo-L-N-methylphenylalanyl-D-N-methylphenylalanyl 
• 94514-47-3 (+/-)-trans-1,4-diacetyl-3,6-dibenzylpiperazine-2,5-dione 
• 59552-68-0 (+/-)-cis-1,4-diacetyl-3,6-dibenzylpiperazine-2,5-dione 
• 133357-48-9 3,6-dibenzyl-2-benzyloxy-5-methoxypyrazine 4-oxide 
• 132213-67-3 3,6-dibenzyl-2-benzyloxy-5-methoxypyrazine 1-oxide 
• 132213-66-2 3,6-dibenzyl-2-benzyloxy-5-methoxypyrazine 
• 132213-63-9 6-(α-acetoxybenzyl)-3-benzyl-5-methoxypyrazine 
• 132213-64-0 2-acetoxy-3,6-dibenzyl-5-methoxypyrazine 
• 117333-12-7 emeheterone 

Relevant academic research and scientific papers

Towards structure determination of self-assembled peptides using dynamic nuclear polarization enhanced solid-state NMR spectroscopy

Supra-sensitivity: Dynamic nuclear polarization (DNP) enhanced solid-state NMR spectroscopy was performed on self-assembled peptide nanotubes. This approach yields significant experimental time savings (about five orders of magnitude; see picture) and was

Biomimetic protecting-group-free 2′, 3′-selective aminoacylation of nucleosides and nucleotides

Aminoacyl phosphate monoesters can be prepared free of an amino-protecting group and used directly in lanthanum-promoted selective monoacylation of either the 2′ or 3′-hydroxyl of nucleosides and nucleotides. For example, phenylalanyl ethyl phosphate rapi

Investigation of reaction mechanism of amino acids and phosphorus trichloride by 31P NMR and ESI-MS/MS

The reaction of amino acids and phosphorus trichloride in THF was studied by 31P NMR tracing and ESI-MS/MS. A series of hydridophoranes and cyclic dipeptides were obtained. The reaction presented interesting diversity and the reaction mechanism was proposed. The mechanism suggests that phosphorus plays an important role in the synthesis of amino acid hydridophorane and cyclic dipeptides. The results also show that 31P NMR and ESI-MS/MS are useful tools for the investigation of reaction mechanism. Copyright

A SYNTHETIC CYCLIC DIPEPTIDE AND A PROCESS THEREOF

The disclosure relates to preparation and self-assembly of aromatic cyclic dipeptide into one and two dimensional nano, meso and micro structures. The said structures of cyclic dipeptide can be electrospinned into threads, fabrics, suture, bandage materials. They are also useful in cell culturing, tissue culturing, drug delivery system, as composite materials, as inhibitors of fibrillization and in Biomedical research such as neurological regeneration and organ replacement studies.

EMEHETERONE: SYNTHESIS AND STRUCTURAL REVISION

Emeheterone, a fungal metabolite, was synthesized from DL-phenylalanine.Based on the results of this synthesis, the structure of emeheterone was redetermined as 3,6-dibenzyl-2-hydroxy-5-methoxypyrazine 4-oxide.

Pyrazine Chemistry. II. Reduction of 3,6-Dibenzylidenepiperazine-2,5-diones

A reinvestigation of the reduction of 3,6-dibenzylidenepiperazine-2,5-dione (1) with zinc and acetic acid established that this reaction gave (Z)-6-benzyl-3-benzylidenepiperazine-2,5-dione (10).When a mixture of acetic acid and hydrochloric acid was used