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2,4-Cyclohexadien-1-one, 6-[5-[2-(phenylmethoxy)phenyl]-3H-1,2,4-dithiazol-3-ylidene]is a complex organic compound featuring a cyclohexadienone core with a dithiazolylidene group attached to it. The molecule is further characterized by the presence of a phenylmethoxyphenyl group connected to the dithiazolylidene ring, resulting in a distinctive molecular architecture. This unique structure may endow the compound with specific properties and reactivity, making it a candidate for applications in various fields such as pharmaceuticals and materials science. Further investigation and research are required to explore the full potential and characteristics of 2,4-Cyclohexadien-1-one, 6-[5-[2-(phenylmethoxy)phenyl]-3H-1,2,4-dithiazol-3-ylidene]-.

138469-98-4

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138469-98-4 Usage

Uses

Used in Pharmaceutical Applications:
2,4-Cyclohexadien-1-one, 6-[5-[2-(phenylmethoxy)phenyl]-3H-1,2,4-dithiazol-3-ylidene]is used as a potential pharmaceutical agent for its unique molecular structure and potential reactivity. 2,4-Cyclohexadien-1-one,
6-[5-[2-(phenylmethoxy)phenyl]-3H-1,2,4-dithiazol-3-ylidene]-'s properties may contribute to the development of new drugs or therapeutic agents, particularly in the context of its interactions with biological systems.
Used in Materials Science Applications:
In the field of materials science, 2,4-Cyclohexadien-1-one, 6-[5-[2-(phenylmethoxy)phenyl]-3H-1,2,4-dithiazol-3-ylidene]is used as a component in the synthesis of novel materials with specific properties. 2,4-Cyclohexadien-1-one,
6-[5-[2-(phenylmethoxy)phenyl]-3H-1,2,4-dithiazol-3-ylidene]-'s structure and reactivity may enable the creation of advanced materials with applications in areas such as electronics, coatings, or other specialized industries.
Used in Research and Development:
2,4-Cyclohexadien-1-one, 6-[5-[2-(phenylmethoxy)phenyl]-3H-1,2,4-dithiazol-3-ylidene]is used as a subject of research in academic and industrial laboratories. 2,4-Cyclohexadien-1-one,
6-[5-[2-(phenylmethoxy)phenyl]-3H-1,2,4-dithiazol-3-ylidene]-'s unique structure and potential reactivity make it an interesting candidate for studies aimed at understanding its properties, reactivity, and potential applications in various fields. This research may lead to the discovery of new uses and applications for the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 138469-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,6 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138469-98:
(8*1)+(7*3)+(6*8)+(5*4)+(4*6)+(3*9)+(2*9)+(1*8)=174
174 % 10 = 4
So 138469-98-4 is a valid CAS Registry Number.

138469-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-<5-(2-Benzyloxyphenyl)-1,2,4-dithiazol-3-yliden>-2,4-cyclohexadien-1-on

1.2 Other means of identification

Product number -
Other names 6-[5-(2-Benzyloxyphenyl)-1,2,4-dithiazol-3-yliden]-2,4-cyclohexadien-1-on

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 -
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More Details:138469-98-4 SDS

138469-98-4Downstream Products

138469-98-4Relevant academic research and scientific papers

Synthesis of heterocyclic immunomodulators. 1. Alkyl derivatives of 1,2,4-dithiazolidin-3,5-diyliden-bis(o-benzoquinone-meth ide): synthesis and testing of immunomodulating action

Briel,Leistner,Droessler

, p. 959 - 961 (2007/10/02)

Reactions of 1,2,4-dithiazolidine-3,5-diylidene-bis(o-benzoquinone-met hid) 3 with alkyl and substituted benzyl or phenacyl halides yield 1,2,4-dithiazol-3-ylidene-quinone-methides 4a-4i. Mass spectral fragmentations of 4a, 4c, and 4f are discussed. Tests

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