N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine
N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine Basic information
- Product Name:
- N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine
- Synonyms:
-
- N6-BENZYL-9-(2-TETRAHYDROPYRANYL)ADENINE (BPA)
- 9-(oxan-2-yl)-N-(phenylmethyl)purin-6-amine
- benzyl-(9-tetrahydropyran-2-ylpurin-6-yl)amine
- 2-(phenylmethyl)-8-(2H-pyran-2-yl)-7H-purin-6-amine
- PYRANYL BENZYLADENINE
- N-(Phenylmethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine
- n-benzyl-9-(tetrahydro-2h-pyran-2-yl)adenine
- N-BENZYL-9-(2'-TETRAHYDROPYRANYL)ADENINE
- CAS:
- 2312-73-4
- MF:
- C17H19N5O
- MW:
- 309.37
- Product Categories:
-
- Plant Hormones
- Mol File:
- 2312-73-4.mol
N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine Chemical Properties
- Melting point:
- 108-110 °C
- Boiling point:
- 449.64°C (rough estimate)
- Density
- 1.0874 (rough estimate)
- refractive index
- 1.7500 (estimate)
- storage temp.
- −20°C
- pka
- 3.51±0.10(Predicted)
- form
- Solid
- color
- White to off-white
- CAS DataBase Reference
- 2312-73-4(CAS DataBase Reference)
- EPA Substance Registry System
- N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine (2312-73-4)
MSDS
- Language:English Provider:SigmaAldrich
N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine Usage And Synthesis
Chemical Properties
White crystals
Uses
N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine is a highly mobile synthetic cytokinin. Foliar spray of N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine increased branching in carnation, chrysan-themum, pointsettia, petunia and fuchsia. Application of N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine to flower buds at an early stage increased both the diameter and the fresh weight of carnation flowers or chrysanthemum infloresences.
Preparation
Dissolve alcohol in PrOH (14 ml). Add TEA (0.95 ml, 6.9 mmol) and 6-chloro-9-(tetrahydropyran-2-yl)purine (1.64 g) to the reaction mixture. Heat the reaction mixture at 45 °C for 6 hours. Cool the reaction mixture. Filter the mixture. Evaporate the filtrate partly. Purify the filtrate by CC (60.3 g of silica gel, mobile phase CHCl3-Me2CO 4:1, flow rate 7.5 ml/min). The product is a light yellow viscous substance that starts to crystallize after two weeks of drying over P2O5 in a vacuum desiccator.
Safety Profile
Moderately toxic by ingestion.Experimental reproductive effects. When heated todecomposition it emits toxic vapors of NOx.
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