35966-95-1

Basic information

• Product Name: N-benzyl-9-cyclopentyl-9H-purin-6-amine
• CAS NO: 35966-95-1
• Molecular Formula: C₁₇H₁₉N₅
• Molecular Weight: 293.3663
• Mol File: 35966-95-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 512.3°C at 760 mmHg
• Flash Point: 263.6°C
• Density: 1.32g/cm³
• Vapor Pressure: 1.31E-10mmHg at 25°C
• Refractive Index: 1.711
• CAS DataBase Reference: N-benzyl-9-cyclopentyl-9H-purin-6-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-9-cyclopentyl-9H-purin-6-amine(35966-95-1)
• EPA Substance Registry System: N-benzyl-9-cyclopentyl-9H-purin-6-amine(35966-95-1)

Safety Data

• Hazardous Substances Data: 35966-95-1(Hazardous Substances Data)

Upstream product

• 5444-81-5 6-chloro-9-cyclopentyl-9H-purine 
• 100-46-9 benzylamine 

Relevant articles and documents

COMPARISON OF CYTOKININ ACTIVITIES OF 9-SUBSTITUTED N6-BENZYLADENINES IN THE CUCUMIS AND AMARANTHUS BIOASSAYS

9-Substituted N6-benzyladenines were tested for their ability to eliminate the lag phase in and promote chlorophyll synthesis in Cucumis sativus cotyledons and for their effectiveness in eliciting the dark biosynthesis of betacyanin in Amaranthus tricolor cotyledon-hypocotyl explants.The following general relationships were established for dose-responses: (a) 9-ribosidation brought about little (in Amaranthus) or no (in Cucumis) decrease in activity relative to the free base, (b) the presence of a 9-ribose 5'-phosphate group moderately depressed activity in Amaranthus but slightly enhanced activity in Cucumis, (c) the presence of a 9-ribose 3',5'-cyclic phosphate group depressed activity substantially in both systems, more so in Amaranthus, (d) 9-glucosylation greatly decreased activity, as did 7-glucosylation, while 3-glucosylation depressed activity to a much lesser extent, in both systems, (e) 9-substitution with cyclopentyl, methyl, methoxymethyl, and tetrahydropyranyl groups reduced activity, the first two substituents more so than the last two, and (f) alteration of the 9-riboside group to a 9- moiety by oxidation-reduction led to complete (in Amaranthus) or nearly complete (in Cucumis) inactivation.Responses to hormone treatment were detectable after dark incubation times as short as 4 hr (in Cucumis) or 8 hr (in Amaranthus). - Key Word Index: Cucumis sativus; Cucurbitaceae; Amaranthus tricolor; Amaranthaceae; cytokinin activity; chlorophyll synthesis; amaranthin synthesis; bioassays; substituted N6-benzyladenines.