34097-37-5

Basic information

• Product Name: N,N'-1H-PURINE-2,6-DIYBIS ACETAMIDE
• Synonyms: N,N'-1H-PURINE-2,6-DIYBIS ACETAMIDE
• CAS NO: 34097-37-5
• Molecular Formula: C₉H₁₀N₆O₂
• Molecular Weight: 234.21
• Mol File: 34097-37-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.585g/cm³
• CAS DataBase Reference: N,N'-1H-PURINE-2,6-DIYBIS ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-1H-PURINE-2,6-DIYBIS ACETAMIDE(34097-37-5)
• EPA Substance Registry System: N,N'-1H-PURINE-2,6-DIYBIS ACETAMIDE(34097-37-5)

Safety Data

• Hazardous Substances Data: 34097-37-5(Hazardous Substances Data)

Usage

General Description

N,N'-1H-PURINE-2,6-DIYBIS ACETAMIDE is a chemical compound that belongs to the purine class. It is a derivative of purine and contains two acetamide groups attached to the 2 and 6 positions of the purine ring. Purines are known for their role in DNA and RNA structure, as well as their involvement in various biochemical processes in the body. N,N'-1H-PURINE-2,6-DIYBIS ACETAMIDE may have potential applications in the pharmaceutical industry, particularly in the development of drugs targeting purine metabolism or related pathways. As with any chemical compound, proper handling and storage protocols should be followed to ensure safety and efficacy in its intended use.

Upstream product

• 93-97-0 benzoic acid anhydride 
• 1904-98-9 2,6-diaminopurine 
• 108-24-7 acetic anhydride 

Downstream Products

• 89419-18-1 6-Amino-9-(2-benzyloxy-1-benzyloxymethyl-ethoxymethyl)-3,9-dihydro-purin-2-one 
• 89419-14-7 9-(2-Benzyloxy-1-benzyloxymethyl-ethoxymethyl)-9H-purine-2,6-diamine 
• 89419-16-9 9-(2-Benzyloxy-1-benzyloxymethyl-ethoxymethyl)-2-fluoro-9H-purin-6-ylamine 
• 89419-15-8 2-(6-Amino-2-fluoro-purin-9-ylmethoxy)-3-benzyloxy-propan-1-ol 
• 82410-32-0 ganciclovir 
• 869355-04-4 N'-[9-((2R,3R,5S)-3-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl]-N,N-dimethyl-formamidine 
• 159217-68-2 N'-(9-{(2R,3R,5S)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-3-hydroxy-tetrahydro-furan-2-yl}-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethyl-formamidine 
• 89419-13-6 N-[2-Acetylamino-9-(2-benzyloxy-1-benzyloxymethyl-ethoxymethyl)-9H-purin-6-yl]-acetamide 
• 114753-52-5 9-(3-azido-2,3-dideoxy-β-D-erythro-pentofuranosyl)-2,6-diaminopurine 
• 121231-92-3 2,6-diamino-9-(3-azido-2,3-dideoxy-α-D-erythro-pentofuranosyl)purine 

Relevant articles and documents

Prolinamides of Aminouracils, Organocatalyst Modifiable by Complementary Modules

We report the synthesis and evaluation of prolinamide organocatalysts that incorporate aminouracils. The features of these catalysts are enhanced NH acidity of the amide because of the electron-withdrawing nature of the heterocycle, an additional hydrogen-bond donor at the α or β positions of this functional group (using 6-aminouracil or 5,6-diaminouracil respectively), and it can be recovered due to its low solubility and used again without decreasing the enantioselectivity. A unique feature of these systems is the self-assembly capability with complementary modules by Watson–Crick interactions. These supramolecular adducts behave differently from the catalyst alone, some of them have lower performance but others improve the selectivity of the product. Therefore, this approach avoids the synthesis of many catalysts.