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[2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenoxy]phosphonic acid is a complex organic chemical compound characterized by the presence of a phosphonic acid group, a methoxy group, and a phenyl group with multiple methoxy substituents. [2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenoxy]phosphonic acid features a Z-configured double bond, which may contribute to its unique properties and potential applications in various fields such as pharmaceuticals, agrochemicals, or materials science. However, further research is necessary to explore its full potential and biological activities.

222030-63-9

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222030-63-9 Usage

Uses

Used in Pharmaceutical Industry:
[2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenoxy]phosphonic acid is used as a potential pharmaceutical agent for its unique structure and properties. [2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenoxy]phosphonic acid may have applications in the development of new drugs or therapeutic agents due to its complex molecular structure and the presence of functional groups that can interact with biological targets.
Used in Agrochemical Industry:
In the agrochemical industry, [2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenoxy]phosphonic acid may be utilized as a potential active ingredient in the development of new pesticides or herbicides. Its unique structure and properties could offer novel modes of action or improved efficacy compared to existing products.
Used in Materials Science:
[2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenoxy]phosphonic acid may also find applications in materials science, where its unique structure and properties could be leveraged to develop new materials with specific characteristics. This could include applications in areas such as polymers, coatings, or advanced materials with tailored properties for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 222030-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,0,3 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 222030-63:
(8*2)+(7*2)+(6*2)+(5*0)+(4*3)+(3*0)+(2*6)+(1*3)=69
69 % 10 = 9
So 222030-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H21O8P/c1-22-14-8-7-12(9-15(14)26-27(19,20)21)5-6-13-10-16(23-2)18(25-4)17(11-13)24-3/h5-11H,1-4H3,(H2,19,20,21)/b6-5-

222030-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenyl] dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names combretastatin A-4 dihydrogen phosphate

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:222030-63-9 SDS

222030-63-9Relevant academic research and scientific papers

Synthesis and antitumor-evaluation of cyclopropyl-containing combretastatin analogs

Fuerst, Rita,Zupko, Istvan,Berenyi, Agnes,Ecker, Gerhard F.,Rinner, Uwe

scheme or table, p. 6948 - 6951 (2010/08/06)

Several derivatives of combretastatin have been prepared bearing a cyclopropyl unit instead of the natural occurring cis-double bond. Final products and synthetic intermediates were evaluated for their cytotoxic properties in two human cancer cell lines.

METHODS OF PREPARING PHOSPHORIC ACIDS OF COMBRETASTATIN AND DERIVATIVES THEREOF

-

Page/Page column 14-15, (2008/12/08)

Methods of synthesizing phosphoric acid of combretastatin A-4, phosphoric acid of combretastatin A-4 derivatives, and trans-isomers thereof are disclosed.

Synthesis of combretastatin A-4 prodrugs and trans-isomers thereof

-

Page/Page column 12, (2008/06/13)

The present invention relates to novel water-soluble, stable derivatives of combretastatin A-4, and novel synthesis methods therefore. The combretastatin A-4 prodrugs described herein appear to be useful in the treatment of neoplastic disease.

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