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6,7-Dimethoxyisoquinoline-1-carbaldehyde is a chemical compound with the molecular formula C12H11NO3. It is a derivative of isoquinoline and contains two methoxy groups at the 6 and 7 positions, as well as an aldehyde group at the 1 position. 6,7-Dimethoxyisoquinoline-1-carbaldehyde has been studied for its potential biological and pharmaceutical applications, including its use as a building block in the synthesis of various organic compounds. It is also of interest for its potential as an intermediate in the synthesis of various pharmaceuticals and natural products. However, its specific properties, potential uses, and any potential hazards associated with its use would depend on the specific context and application.

71046-35-0

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71046-35-0 Usage

Uses

Used in Pharmaceutical Industry:
6,7-Dimethoxyisoquinoline-1-carbaldehyde is used as a building block for the synthesis of various organic compounds, particularly in the development of new pharmaceuticals and natural products. Its unique structure and functional groups make it a valuable intermediate in the creation of novel therapeutic agents.
Used in Organic Synthesis:
6,7-Dimethoxyisoquinoline-1-carbaldehyde is used as a key intermediate in the synthesis of complex organic molecules. Its presence in the molecule allows for further functionalization and modification, enabling the development of a wide range of chemical entities with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 71046-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,4 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71046-35:
(7*7)+(6*1)+(5*0)+(4*4)+(3*6)+(2*3)+(1*5)=100
100 % 10 = 0
So 71046-35-0 is a valid CAS Registry Number.

71046-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-dimethoxyisoquinoline-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-formyl 6,7-dimethoxy isoquinoline

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:71046-35-0 SDS

71046-35-0Relevant academic research and scientific papers

Total Synthesis of Aaptamine, Demethyloxyaaptamine, and Their 3-Alkylamino Derivatives

Gao, Yuan,Yang, Fan,Sun, Fan,Liu, Lei,Liu, Bo,Wang, Shu-Ping,Cheng, Chun-Wei,Liao, Hongze,Lin, Hou-Wen

, p. 1430 - 1433 (2019)

A simple and efficient synthetic route for preparing the benzonaphthyridine framework is reported. Only seven steps are needed for the assembly of 3-alkylamino aaptamine from inexpensive isoquinoline 6 by this route with about 20% overall yield. The two k

A SYNTHESIS OF AAPTAMINE FROM 6,7-DIMETHOXY-1-METHYLISOQUINOLINE

Batczewski, Piotr,Mallon, M. Kieran J.,Street, Jonathan D.,Joule, John A.

, p. 3193 - 3198 (2007/10/02)

6,7-Methoxy-1-methylisoquinoline 3a was nitratwd at C-8, oxidised to thenitro aldehyde 3r and then condensed with nitromethane using alumina as base to give the alcohol 3s, dehydration of which produced the nitroethene 3t.Iron-acetic acid treatment of com

Oxydation vanadique de la papaverine en milieu sulfurique 2,5 M et 5 M

Postaire, E.,Martinez, D.,Viel, C.,Chastagnier, M.,Hamon, M.

, p. 982 - 988 (2007/10/02)

Vanadic oxidation of papaverine 1 in 5 M sulfuric acid media shows a full oxidation into carbon dioxide and water.However, according to the experimental conditions, and in 2.5 M and 5 M sulfuric acid media, intermediates and products have been identified: papaveraldine 2, hemipinimide 4, meta-hemipinic acid 3, 6,7-dimethoxy isoquinoline 5, 1-formyl 6,7-dimethoxy isoquinoline 6, 1-acetyl 6,7-dimethoxy isoquinoline 7, 4-hydroxy 6-demethyl papaveraldine 8, 4-hydroxy 4'demethyl papaveraldine 9, 3-hydroxy 6-demethyl papaveraldine 10 and 3-hydroxy 4'-demethyl papaveraldine 11.

Isoquinoline propionamides exhibiting analgesic properties

-

, (2008/06/13)

Disclosed are novel isoquinoline propionamides and their acid salts represented by the structural formula: STR1 wherein R is alkyl of 1 to 6 carbon atoms, methylcycloalkyl of 4 to 7 carbon atoms or alkaryl of 7 to 8 carbon atoms; R' is H or OCH3/sub

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