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Usage

Uses

Used in Plant Biotechnology:
N2-acetamido-6-benzyloxypurine is used as a growth regulator for promoting cell division and differentiation in plant tissue cultures. It is particularly effective in stimulating the proliferation of shoot and root cultures, leading to increased biomass production and improved quality of plant tissue.
Used in Agricultural Research:
N2-acetamido-6-benzyloxypurine is used as a plant growth enhancer for improving the overall growth and development of various plant species. It has been shown to effectively delay senescence and promote the formation of lateral shoots and roots, making it a valuable tool in agricultural research for optimizing plant growth and productivity.
Used in Tissue Culture Systems:
N2-acetamido-6-benzyloxypurine is used as a cytokinin plant hormone in tissue culture systems to stimulate the growth and development of plant cells. Its ability to activate specific cellular pathways that regulate cell division and differentiation makes it an essential component in the development of efficient and effective tissue culture techniques for plant propagation and improvement.

Upstream product

• 100-51-6 benzyl alcohol 
• 133310-37-9 guanine 
• 10310-21-1 2-Amino-6-chloropurin 
• 108-24-7 acetic anhydride 
• 19916-73-5 2-Amino-6-benzyloxypurine 

Downstream Products

• 160363-14-4 N-[6-Benzyloxy-9-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-9H-purin-2-yl]-acetamide 
• 189829-42-3 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-6-(2-acetylamino-6-benzyloxy-purin-9-yl)-5-(2,2,2-trifluoro-acetylamino)-tetrahydro-pyran-4-yl ester 

Relevant academic research and scientific papers

Rapid Entry into Biologically Relevant α,α-Difluoroalkylphosphonates Bearing Allyl Protection-Deblocking under Ru(II)/(IV)-Catalysis

A convenient synthetic route to α,α-difluoroalkylphosphonates is described. Structurally diverse aldehydes are condensed with LiF2CP(O)(OCH2CH-CH2)2. The resultant alcohols are captured as the pentafluorophenyl thionocarbonates and efficiently deoxygenated with HSnBu3, BEt3, and O2, and then smoothly deblocked with CpRu(IV)(π-allyl)quinoline-2-carboxylate (1-2 mol %) in methanol as an allyl cation scavenger. These mild deprotection conditions provide access to free α,α-difluoroalkylphosphonates in nearly quantitative yield. This methodology is used to rapidly construct new bis-α,α-difluoroalkyl phosphonate inhibitors of PTPIB (protein phosphotyrosine phosphatase-1B).

An unusual solvent effect on the regiochemical outcome (N-9 versus N-7) of guanine glycosylation using Robins' reagent (2-N-acetyl-6-O- diphenylcarbamoylguanine)

An unexpectedly low N-9/N-7 regioselectivity was obtained when Robins reagent (2-N-acetyl-6-O-diphenylcarbamoylguanine) was coupled with a D- glucosamine derivative under trimethylsilyl trifluoromethanesulfonate activation. An unprecedented solvent effect (toluene versus dichloroethane) on the N-9/N-7 ratio was also observed in the same study. The use of 2-N- acetyl-6-O-benzylguanine to successfully overcome the above regioselectivity problem is described. (C) 2000 Elsevier Science Ltd.