269-44-3

Basic information

• Product Name: [1,3]DIOXOLO[4,5-G]ISOQUINOLINE
• Synonyms: [1,3]DIOXOLO[4,5-G]ISOQUINOLINE
• CAS NO: 269-44-3
• Molecular Formula: C₁₀H₇NO₂
• Molecular Weight: 173.17
• Mol File: 269-44-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 127-128 °C
• Boiling Point: 333.2±11.0 °C(Predicted)
• Appearance: /
• Density: 1.353±0.06 g/cm3(Predicted)
• PKA: 6.25±0.20(Predicted)
• CAS DataBase Reference: [1,3]DIOXOLO[4,5-G]ISOQUINOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: [1,3]DIOXOLO[4,5-G]ISOQUINOLINE(269-44-3)
• EPA Substance Registry System: [1,3]DIOXOLO[4,5-G]ISOQUINOLINE(269-44-3)

Safety Data

• Hazardous Substances Data: 269-44-3(Hazardous Substances Data)

Usage

General Description

[1,3]Dioxolo[4,5-g]isoquinoline is a heterocyclic compound with a unique chemical structure. It belongs to the class of organic compounds known as isoquinolines, which are aromatic compounds containing a benzene ring fused to a pyridine ring. [1,3]DIOXOLO[4,5-G]ISOQUINOLINE is highly reactive due to the presence of the dioxolo ring, and it may be used as a building block in organic synthesis. It has potential applications in pharmaceuticals, agrochemicals, and materials science due to its ability to form biologically active compounds and functional materials. Additionally, [1,3]Dioxolo[4,5-g]isoquinoline derivatives have shown interesting biological activities, making them promising candidates for drug discovery and development. Overall, this compound has various potential applications and is an important target for synthetic chemists and researchers in the field of medicinal chemistry.

Upstream product

• 53012-84-3 2-formyl-4,5-dimethoxybenzoic acid methyl ester 
• 39964-98-2 2-benzoyl-6,7-methylenedioxy-1,2-dihydroisoquinoline-1-carbonitrile 
• 4122-56-9 methyl o-formylbenzoate 
• 94143-83-6 5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline 

Downstream Products

• 17656-61-0 (6,7-methylenedioxyisoquinolinyl)-(4'-methoxyphenyl)-methanone 
• 475-75-2 liriodenine 
• 87489-85-8 (2-bromophenyl)([1,3]dioxolo[4,5-g]isoquinolin-5-yl)methanone 
• 39964-98-2 2-benzoyl-6,7-methylenedioxy-1,2-dihydroisoquinoline-1-carbonitrile 
• 38699-63-7 5-(4-benzyloxy-3-methoxy-benzyl)-[1,3]dioxolo[4,5-g]isoquinoline 
• 38750-42-4 6-benzoyl-5-(3-benzyloxy-4-methoxy-benzyl)-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinoline-5-carbonitrile 
• 16658-48-3 Escholamin 
• 494-55-3 N-methyl-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline 
• 123796-55-4 O-benzylberbithine 
• 105798-91-2 berbithine 
• 70400-40-7 1-(3-hydroxy-4-methoxybenzyl)-6,7-methylenedioxyisoquinoline 
• 38750-43-5 O-benzylisosevanine 
• 627884-05-3 6-[[5,6-dihydro-8,9-methylenedioxy-1-oxo-3-phenyloxazolo[4,3-a]isoquinolin-10b-yl]methyl]-2,3-dimethoxybenzoic acid ethyl ester 
• 627884-07-5 6-[[5,6-dihydro-8,9-methylenedioxy-1-oxo-3-phenyloxazolo[4,3-a]isoquinolin-10b-yl]methyl]-2,3-methylenedioxybenzoic acid ethyl ester 

Relevant articles and documents

Radical-mediated Synthesis of the 5,11-Methanomorphanthridine Ring System: Formal Total Synthesis of Montanine-type Amaryllidaceae Alkaloids, (+/-)-Montanine, (+/-)-Coccinine and (+/-)-Pancracine

Radical-mediated reaction of the phenyl sulfide 16 and the phenyl selenide 17 in boiling toluene or o-xylene containing AIBN gave, in moderate yields, the 5,11-methanomorphanthridine ring system 4, which is a basic skeleton of montanine-type Amaryllidacea

Central nervous system active compounds. VI. Reissert compounds as precursors of 1-(3-phthalidyl)isoquinolines

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