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1,3-Dioxolo[4,5-f]isoquinoline is a heterocyclic organic compound characterized by a fused ring structure consisting of an isoquinoline ring and a dioxolo ring. 1,3-Dioxolo[4,5-f]isoquinoline is a tricyclic aromatic system with the molecular formula C11H7NO2. It is an important intermediate in the synthesis of various pharmaceuticals and natural products, such as alkaloids, due to its unique structure and reactivity. The presence of both nitrogen and oxygen atoms in the molecule allows for a wide range of chemical transformations, making it a valuable building block in organic synthesis. The compound can be synthesized through various methods, including cyclization reactions and condensation processes, and is often used as a precursor in the preparation of more complex molecules with potential biological activities.

234-16-2

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234-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 234-16-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 234-16:
(5*2)+(4*3)+(3*4)+(2*1)+(1*6)=42
42 % 10 = 2
So 234-16-2 is a valid CAS Registry Number.

234-16-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [1,3]dioxolo[4,5-f]isoquinoline

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:234-16-2 SDS

234-16-2Downstream Products

234-16-2Relevant academic research and scientific papers

Isoquinoline synthesis by C-H activation/annulation using vinyl acetate as an acetylene equivalent

Webb, Nicola J.,Raw, Steven A.,Marsden, Stephen P.

, p. 5200 - 5205 (2018/06/19)

Vinyl acetate is used as an acetylene equivalent in rhodium(III)-catalysed C-H activation/annulation with aryl ketoxime esters. Extension to an aldoxime ester allows for a concise formal synthesis of decumbenine B.

Synthesis of a 3-arylisoquinoline alkaloid, decumbenine B

Wada, Yasuhiro,Nishida, Naoto,Kurono, Nobuhito,Ohkuma, Takashi,Orito, Kazuhiko

, p. 4320 - 4327 (2008/03/18)

The synthesis of a 3-arylisoquinoline alkaloid, decumbenine B, was accomplished in a reaction sequence based on the formation of an indolizine ring (dibenz[a,f]indolizin-5(7H)-one) followed by its cleavage at the amide bond, starting with an interaction o

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