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1,3(2H,4H)-Isoquinolinedione, 4-(1-methylethyl)-2-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

190579-12-5

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190579-12-5 Usage

Pharmaceutical Properties

Proglumide has properties that make it useful in the medical field.

Cholecystokinin Antagonist

Proglumide can block the effects of cholecystokinin, a hormone that regulates appetite and digestion.

Involvement in Digestion

By blocking cholecystokinin, Proglumide can potentially influence digestion.

Treatment of Gastrointestinal Disorders

Proglumide has been studied for its potential use in treating conditions like peptic ulcers and dyspepsia.

Peptic Ulcers

Open sores that develop in the lining of the stomach, duodenum, or esophagus.

Dyspepsia

A chronic or recurrent pain or discomfort in the upper abdomen, also known as indigestion.

Potential for Weight Management

Proglumide has been investigated for its potential to reduce food intake and aid in weight management.

Gastroenterology and Obesity Research

Proglumide shows promise in these fields due to its effects on appetite and digestion.

Structure

The compound has a complex structure involving isoquinolinedione, a 1-methylethyl group, and a phenylmethyl group.

Chemical Classification

Proglumide can be classified based on its structure, function, and the biological systems it interacts with.

Synonyms

Proglumide may have other names or synonyms used in different contexts or regions.

Dosage and Administration

The appropriate dosage and method of administration for Proglumide in medical treatments would need to be determined through research and clinical trials.

Side Effects and Safety

As with any pharmaceutical compound, the potential side effects and safety of Proglumide should be carefully studied and considered.

Regulatory Status

The approval and regulation of Proglumide for medical use would depend on the results of clinical trials and the decisions of relevant health authorities.

Intellectual Property

The patent status and ownership of Proglumide could impact its development, production, and distribution.

Manufacturing Process

The method of synthesizing Proglumide, including the starting materials, reaction conditions, and purification techniques.

Stability and Storage

Information on the stability of Proglumide under various conditions and the recommended storage methods to maintain its efficacy and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 190579-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,5,7 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 190579-12:
(8*1)+(7*9)+(6*0)+(5*5)+(4*7)+(3*9)+(2*1)+(1*2)=155
155 % 10 = 5
So 190579-12-5 is a valid CAS Registry Number.

190579-12-5SDS

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 2-benzyl-4-propan-2-yl-4H-isoquinoline-1,3-dione

1.2 Other means of identification

Product number -
Other names 1,3(2H,4H)-Isoquinolinedione,4-(1-methylethyl)-2-(phenylmethyl)

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:190579-12-5 SDS

190579-12-5Downstream Products

190579-12-5Relevant academic research and scientific papers

The oxidation of homophthalimide derivatives by dioxygen in alkaline media and cleavage-cyclisation reactions

Heaney, Harry,Taha, Mutasem O.,Slawin, Alexandra M. Z.

, p. 3051 - 3054 (1997)

The oxidation of α-alkylhomophthalimide derivatives by dioxygen in the presence of ethanolic sodium hydroxide leads to the rapid formation of α-hydroxy-α-alkylhomophthalimide derivatives and hence, as a result of ring cleavage and lactone formation, to α-amido-α-alkylphthalides, potential precursors to phthalide isoquinoli ne alkaloids and analogues.

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