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523-80-8

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523-80-8 Usage

Description

4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE is an organic compound characterized by its unique molecular structure, which features a benzene ring with two oxygen atoms connected to it, forming a dioxole ring. 4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE also has two methoxy groups attached to the 4th and 7th carbon atoms, and a propanyl group connected to the 5th carbon atom. This structure endows the compound with various chemical and biological properties, making it a versatile molecule for different applications.

Uses

Used in Pharmaceutical Industry:
4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE is used as an active pharmaceutical ingredient for its potential therapeutic effects. 4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE's unique structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs to treat various diseases.
Used in Chemical Industry:
In the chemical industry, 4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE can be used as a building block or intermediate in the synthesis of more complex organic molecules. Its versatile structure allows for further functionalization and modification, enabling the creation of a wide range of chemical products.
Used in Agricultural Industry:
4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE is used as an insecticide due to its potential to disrupt the nervous system of insects, leading to their paralysis and eventual death. This application can help in controlling pest populations and protecting crops from damage.
Used in Antipyretic Applications:
4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE can be used as an antipyretic, helping to reduce fever and alleviate the discomfort associated with elevated body temperatures. Its cooling effect can be beneficial in managing symptoms during illnesses.
Used in Diuretic Applications:
4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE can also be employed as a diuretic, promoting the increased production and excretion of urine. This can be useful in treating conditions related to fluid retention and high blood pressure.
Used in Antinociceptive and Anti-inflammatory Applications:
Similar to Apioline, 4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE may exhibit antinociceptive and anti-inflammatory properties, making it a potential candidate for the development of pain relief and anti-inflammatory medications. Its ability to alleviate pain and reduce inflammation can be beneficial in managing various conditions, such as arthritis and other inflammatory disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 523-80-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 523-80:
(5*5)+(4*2)+(3*3)+(2*8)+(1*0)=58
58 % 10 = 8
So 523-80-8 is a valid CAS Registry Number.

523-80-8SDS

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 Apiole

1.2 Other means of identification

Product number -
Other names Parsley apiol

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:523-80-8 SDS

523-80-8Relevant articles and documents

Rhodium- and iridium-catalyzed allylation of electron-rich arenes with allyl tosylate

Tsukada, Naofumi,Yagura, Yasushige,Sato, Tetsuo,Inoue, Yoshio

, p. 1431 - 1434 (2007/10/03)

The allylation of electron-rich arenes with allyl tosylate proceeded at 0°C in the presence of [Rh(nbd)(CH3CN)2]PF 6. Various oxygenated arenes were allylated with high para-selectivity in almost all cases. Especially in t

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