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7-methoxy-2-methylisoquinoline-1,3(2H,4H)-dione is a chemical compound with the molecular formula C12H11NO3. It is a derivative of isoquinoline and contains a methoxy and a methyl group. 7-methoxy-2-methylisoquinoline-1,3(2H,4H)-dione has potential pharmaceutical applications and is being studied for its pharmacological properties, including its potential as an anticancer and antifungal agent. It is also being researched for its potential as a fluorescent probe in biological imaging applications. Additionally, 7-methoxy-2-methylisoquinoline-1,3(2H,4H)-dione has been found to have antioxidant and anti-inflammatory properties, making it of interest for further research and potential development as a therapeutic agent.

76746-95-7

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76746-95-7 Usage

Uses

Used in Pharmaceutical Industry:
7-methoxy-2-methylisoquinoline-1,3(2H,4H)-dione is used as a potential anticancer agent for its pharmacological properties that may help in the treatment of cancer.
7-methoxy-2-methylisoquinoline-1,3(2H,4H)-dione is used as a potential antifungal agent for its ability to combat fungal infections.
Used in Biomedical Research:
7-methoxy-2-methylisoquinoline-1,3(2H,4H)-dione is used as a fluorescent probe in biological imaging applications for its potential to enhance visualization of cellular structures and processes.
Used in Antioxidant and Anti-inflammatory Applications:
7-methoxy-2-methylisoquinoline-1,3(2H,4H)-dione is used as a therapeutic agent for its antioxidant and anti-inflammatory properties, which may contribute to the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 76746-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,4 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76746-95:
(7*7)+(6*6)+(5*7)+(4*4)+(3*6)+(2*9)+(1*5)=177
177 % 10 = 7
So 76746-95-7 is a valid CAS Registry Number.

76746-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-N-methylhomophthalimide

1.2 Other means of identification

Product number -
Other names 7-methoxy-2-methyl-4H-isoquinoline-1,3-dione

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:76746-95-7 SDS

76746-95-7Downstream Products

76746-95-7Relevant academic research and scientific papers

Isoquinolones: Part IV - Synthesis of 3-Methylisoquinolone-4-carboxylic Acids and Action of Ammonia and Aqueous Methyl Amine on 3-Methylisocoumarin-4-carboxylic Acid Esters

Datta, D.,Tirodkar, R. B.,Usgaonkar, R. N.

, p. 641 - 643 (2007/10/02)

Ammonia reacts with 3-methylisocoumarin-4-carboxylic acid ester (II) on a boiling water-bath to give homophthalimide (III, R'=H) and 3-methylisoquinolone-4-carboxylic acid ester (IV) in nearly equal amounts.At room temperature ammonia reacts to give IV as the major product in good yield.Aq. methyl amine, however, reacts with II to give N-methylhomophthalimide (III, R'=Me) as the major product along with small amounts of compound VI (R1=Me) and some unchanged isocoumarin.Formation of the various products has been rationalised.

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