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1309478-07-6

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1309478-07-6 Usage

General Description

Wittifuran X is a natural chemical compound found in the Wittigia fischeri plant. It is a furan derivative and has been isolated from the roots and aerial parts of the plant. Wittifuran X has been the subject of research for its potential pharmacological properties, including its antiproliferative, anti-inflammatory, and cytotoxic effects. It has also shown promise in inhibiting the growth of cancer cells in various studies. The compound has attracted attention from the scientific community for its potential medicinal uses and continues to be studied for its biological activities and therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 1309478-07-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,4,7 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1309478-07:
(9*1)+(8*3)+(7*0)+(6*9)+(5*4)+(4*7)+(3*8)+(2*0)+(1*7)=166
166 % 10 = 6
So 1309478-07-6 is a valid CAS Registry Number.

1309478-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Wittifuran X

1.2 Other means of identification

Product number -
Other names -

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:1309478-07-6 SDS

1309478-07-6Upstream product

1309478-07-6Downstream Products

1309478-07-6Relevant articles and documents

Deconstructive Reorganization: De Novo Synthesis of Hydroxylated Benzofuran

Cao, Tongxiang,Jiang, Huanfeng,Zhang, Ling,Zhu, Shifa

, p. 4670 - 4677 (2020/02/20)

An unprecedented deconstructive reorganization strategy for the de novo synthesis of hydroxylated benzofurans from kojic acid- or maltol-derived alkynes is reported. In this reaction, both the benzene and furan rings were simultaneously constructed, whereas the pyrone moiety of the kojic acid or maltol was deconstructed and then reorganized into the benzene ring as a six-carbon component. Through this strategy, at least one free hydroxyl group was introduced into the benzene ring in a substitution-pattern tunable fashion without protection–deprotection and redox adjustment. With this method, a large number of hydroxylated benzofuran derivatives with different substitution-patterns have been prepared efficiently. This methodology has also been shown as the key step in a collective total synthesis of hydroxylated benzofuran-containing natural products (11 examples).

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