525-80-4

Basic information

• Product Name: N-(2-furylmethyl)-7H-purin-6-amine
• Synonyms: N-(2-furylmethyl)-7H-purin-6-amine;2-furylmethyl(7H-purin-6-yl)amine
• CAS NO: 525-80-4
• Molecular Formula: C10H9N5O
• Molecular Weight: 0
• Mol File: 525-80-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-furylmethyl)-7H-purin-6-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-furylmethyl)-7H-purin-6-amine(525-80-4)
• EPA Substance Registry System: N-(2-furylmethyl)-7H-purin-6-amine(525-80-4)

Safety Data

• Hazardous Substances Data: 525-80-4(Hazardous Substances Data)

Upstream product

• 617-89-0 furan-2-ylmethanamine 
• 87-42-3 6-chloro-7H-purine 
• 50-66-8 6-(methylthio)-1H-purine 
• 4316-99-8 N⁴-furfuryl-5-nitro-pyrimidine-4,6-diyldiamine 
• 102236-06-6 N⁴-furfuryl-pyrimidine-4,5,6-triyltriamine 
• 73-24-5 7H-purin-6-ylamine 
• 527-69-5 2-furancarbonyl chloride 
• 958-09-8 2'-deoxy-D-adenosine 
• 533-67-5 2-Deoxy-D-ribose 
• 98-00-0 (2-furyl)methyl alcohol 
• 617-88-9 2-Chloromethylfuran 
• 112299-36-2 N⁴-furfuryl-pyrimidine-4,5,6-triyltriamine; sulfate 
• 77287-34-4 formamide 
• 103647-66-1 N-furfuryl-N-(7⁽⁹⁾H-purin-6-yl)-acetamide 

Downstream Products

• 4338-47-0 kinetin riboside 

Relevant articles and documents

Synthetic method for high-purity 6-furfurylaminopurine

The invention discloses a synthetic method for high-purity 6-furfurylaminopurine. According to the synthetic method, in the existence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), furfuryl amine and 6-chloropurine are subjected to nucleophilic substitution reaction under reflux condition of hexamethyldisilazane so as to obtain a crude product of 6-furfurylaminopurine, and recrystallizing is carriedout so as to obtain 6-furfurylaminopurine, the HPLC purity is 99.5% or above, and the any individual impurity content is less than 0. 1wt%. The synthetic method has the advantages of being simple inprocess, high in yield and free of wastewater discharge.

An efficient direct amination of cyclic amides and cyclic ureas

An efficient one-step amination of cyclic amides and ureas has been developed. Treatment of cyclic amides and cyclic ureas with BOP in the presence of DBU in various solvents led to the formation of cyclic amidines and cyclic guanidines in good to excellent yields. Concise syntheses of biologically intriguing kinetin and potent kinase inhibitor olomoucin were thus achieved in just one and two steps, respectively.