Welcome to LookChem.com Sign In|Join Free

CAS

  • or

63194-69-4

Post Buying Request

63194-69-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

63194-69-4 Usage

Description

(6Z)-6-(3-phenylprop-2-en-1-ylidene)-1,3-benzodioxol-5(6H)-one, commonly known as asarinin, is a naturally occurring organic compound that belongs to the benzodioxole class. It is derived from various plant species, particularly those within the Asarum genus and the seeds of Abelmoschus esculentus. Asarinin has garnered attention for its potential pharmacological properties, which include anti-inflammatory, antioxidant, and neuroprotective effects. Additionally, it has been studied for its possible antitumor activity, making its chemical structure and properties of interest to researchers in medicinal chemistry and phytochemistry.

Uses

Used in Pharmaceutical Applications:
Asarinin is used as a potential therapeutic agent for various conditions due to its anti-inflammatory, antioxidant, and neuroprotective properties. It is being investigated for its ability to alleviate inflammation, counteract oxidative stress, and protect neurons from damage, which could be beneficial in treating a range of diseases and disorders.
Used in Antitumor Applications:
Asarinin is also being explored for its potential antitumor activity. It may be used as a compound in the development of new cancer treatments, particularly if its antitumor properties can be effectively harnessed and delivered to target cancer cells.
Used in Medicinal Chemistry Research:
Asarinin's unique chemical structure and properties make it a valuable subject for further research in medicinal chemistry. Scientists are interested in understanding its mechanisms of action and how it can be modified or used in the development of new drugs with improved efficacy and fewer side effects.
Used in Phytochemistry Studies:
In the field of phytochemistry, asarinin is used as a key compound for studying the chemical constituents of plants from the Asarum genus and Abelmoschus esculentus. Understanding the properties and potential applications of asarinin can contribute to the broader knowledge of plant-based medicines and their therapeutic uses.

Check Digit Verification of cas no

The CAS Registry Mumber 63194-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,9 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63194-69:
(7*6)+(6*3)+(5*1)+(4*9)+(3*4)+(2*6)+(1*9)=134
134 % 10 = 4
So 63194-69-4 is a valid CAS Registry Number.

63194-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (6Z)-6-[(E)-3-phenylprop-2-enylidene]-1,3-benzodioxol-5-one

1.2 Other means of identification

Product number -
Other names OBTUSAQUINONE DERIV JURD 2155

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:63194-69-4 SDS

63194-69-4Upstream product

63194-69-4Relevant articles and documents

Highly Regio-, Diastereo-, and Enantioselective Synthesis of Tetrahydroazepines and Benzo[b]oxepines through Palladium-Catalyzed [4+3] Cycloaddition Reactions

Trost, Barry M.,Zuo, Zhijun

, p. 1243 - 1247 (2020)

A novel Pd0-catalyzed asymmetric [4+3] annulation reaction of two readily accessible starting materials has been developed for building seven-membered heterocyclic architectures. The potential [3+2] side pathway could be suppressed though fine tuning of the conditions. A broad scope of cycloaddition donors and acceptors participated in the transformation with excellent chemo-, regio-, diastereo-, and enantioselectivtities, leading to valuable tetrahydroazepines and benzo[b]oxepines.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 63194-69-4