1501-13-9

Basic information

• Product Name: 7-PHENYL-2,4,9-TRIAZABICYCLO[4.3.0]NONA-1,3,5,7-TETRAEN-5-AMINE
• Synonyms: 7-PHENYL-2,4,9-TRIAZABICYCLO[4.3.0]NONA-1,3,5,7-TETRAEN-5-AMINE;7-Deaza-7-phenyladenine
• CAS NO: 1501-13-9
• Molecular Formula: C₁₂H₁₀N₄
• Molecular Weight: 0
• Mol File: 1501-13-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.348g/cm³
• Refractive Index: 1.75
• CAS DataBase Reference: 7-PHENYL-2,4,9-TRIAZABICYCLO[4.3.0]NONA-1,3,5,7-TETRAEN-5-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 7-PHENYL-2,4,9-TRIAZABICYCLO[4.3.0]NONA-1,3,5,7-TETRAEN-5-AMINE(1501-13-9)
• EPA Substance Registry System: 7-PHENYL-2,4,9-TRIAZABICYCLO[4.3.0]NONA-1,3,5,7-TETRAEN-5-AMINE(1501-13-9)

Safety Data

• Hazardous Substances Data: 1501-13-9(Hazardous Substances Data)

Usage

General Description

7-PHENYL-2,4,9-TRIAZABICYCLO[4.3.0]NONA-1,3,5,7-TETRAEN-5-AMINE is a chemical compound that belongs to the class of triazabicyclo nonane derivatives. It is a bicyclic amine with a phenyl group attached to the 7th position. 7-PHENYL-2,4,9-TRIAZABICYCLO[4.3.0]NONA-1,3,5,7-TETRAEN-5-AMINE has potential pharmacological properties and may be used in medicinal chemistry research. Its specific biological activities and potential therapeutic applications are yet to be fully explored, making it a subject of interest for further study and development in the field of pharmaceutical research.

InChI:InChI=1/C12H10N4/c13-11-10-9(8-4-2-1-3-5-8)6-14-12(10)16-7-15-11/h1-7H,(H3,13,14,15,16)

Upstream product

• 1207543-30-3 4‐chloro‐5‐iodo‐7‐((2‐(trimethylsilyl)ethoxy)methyl)‐7H‐pyrrolo[2,3‐d]pyrimidine 
• 1207543-31-4 5-iodo-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine 
• 123148-78-7 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine 
• 141-52-6 sodium ethanolate 
• 70-11-1 α-bromoacetophenone 
• 613-89-8 2-Aminoacetophenone 
• 54153-51-4 2-amino-3-cyano-4-phenylpyrrole 
• 1816-88-2 2-azido-1-phenylethan-1-one 
• 1846-33-9 N-phenacylacetamide 
• 344359-57-5 N-(3-cyano-4-phenyl-1H-pyrrol-2-yl)-formamidine 

Downstream Products

• 871672-01-4 4-amino-5-phenyl-7-(benzoyloxyethoxymethyl)pyrrolo[2,3-d]pyrimidine 
• 871671-50-0 4-amino-5-phenyl-7-(5-deoxy-2,3-O-isopropylidenyl-β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine 
• 197525-60-3 (2R/4S)-4-4-Amino-5-phenyl-pyrrolo[2,3-d]pyrimidin-7-yl-pyrrolidine-1,2di-carboxylic acid 1-tert-butyl ester 2-ethyl ester 
• 871671-55-5 4-N-(carbomethoxymethyl)amino-5-phenyl-7-(tert-butyldimethylsilyloxyethoxymethyl)pyrrolo[2,3-d]pyrimidine 
• 871671-51-1 4-amino-5-phenyl-7-(tert-butyldimethylsilyloxyethoxymethyl)pyrrolo[2,3-d]pyrimidine 
• 196964-16-6 2-(4-amino-5-phenyl-pyrrolo[2,3-d]pyrimidin-7-ylmethoxy)-ethanol 

Relevant articles and documents

Synthesis of 2,6-Substituted 7-(Het)aryl-7-deazapurine Nucleobases (2,4-Disubstituted 5-(Het)aryl-pyrrolo[2,3- d ]pyrimidines)

A series of 7-(het)aryl-7-deazapurine nucleobases (5-[(het)aryl]-2,4-disubstituted 7 H -pyrrolo[2,3- d ]pyrimidines) bearing NH 2, OMe, SMe, or Me groups at position 6 and H, NH 2, or Me at position 2 were prepared by the aqueous Suzuki-Miyaura cross-coupling reactions from SEM-protected 7-iodo-7-deazapurines with (het)arylboronic acids followed by deprotection. The 6-methoxy derivatives were further transformed into 7-deazahypoxanthines or 7-deazaguanines by O -demethylation reactions. Unlike their ribonucleoside counterparts, the 7-deazapurine nucleobases did not exert any significant cytostatic or antiviral effects.

N-7-HETEROCYCLYL PYRROLO[2,3-D]PYRIMIDINES AND THE USE THEREOF

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