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102565-09-3

(2E)-2-(hydroxy[(E)-2-phenyl-2-thiophen-2-ylethenyl]aminomethylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one is a complex organic molecule with a benzothiophene core, a trifluoromethyl group, and a hydroxy functionality. It also features a substituted amino group and a double bond, giving it a distinct structure. (2E)-2-(hydroxy[(E)-2-phenyl-2-thiophen-2-ylethenyl]aminomethylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one may have potential applications in medicinal chemistry or materials science due to its unique combination of functional groups and stereochemistry.

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  • 102565-09-3 Structure

  • Basic information

    1. Product Name: (2E)-2-(hydroxy{[(E)-2-phenyl-2-thiophen-2-ylethenyl]amino}methylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one
    2. Synonyms:
    3. CAS NO:102565-09-3
    4. Molecular Formula: C22H14F3NO2S2
    5. Molecular Weight: 445.4773
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102565-09-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 532.5°C at 760 mmHg
    3. Flash Point: 275.8°C
    4. Appearance: N/A
    5. Density: 1.462g/cm3
    6. Vapor Pressure: 3.61E-12mmHg at 25°C
    7. Refractive Index: 1.666
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (2E)-2-(hydroxy{[(E)-2-phenyl-2-thiophen-2-ylethenyl]amino}methylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: (2E)-2-(hydroxy{[(E)-2-phenyl-2-thiophen-2-ylethenyl]amino}methylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one(102565-09-3)
    12. EPA Substance Registry System: (2E)-2-(hydroxy{[(E)-2-phenyl-2-thiophen-2-ylethenyl]amino}methylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one(102565-09-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 102565-09-3(Hazardous Substances Data)

102565-09-3 Usage

Uses

Used in Medicinal Chemistry:
(2E)-2-(hydroxy[(E)-2-phenyl-2-thiophen-2-ylethenyl]aminomethylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one is used as a potential pharmaceutical candidate for the development of new drugs. Its unique structure and functional groups may allow for the modulation of biological targets and pathways, leading to the discovery of novel therapeutic agents.
Used in Materials Science:
(2E)-2-(hydroxy[(E)-2-phenyl-2-thiophen-2-ylethenyl]aminomethylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one is used as a building block for the synthesis of new materials with specific properties. Its combination of functional groups and stereochemistry may contribute to the development of advanced materials with applications in various industries, such as electronics, coatings, or polymers.
However, it is important to note that further research and characterization would be necessary to fully understand the properties and potential uses of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 102565-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,6 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102565-09:
(8*1)+(7*0)+(6*2)+(5*5)+(4*6)+(3*5)+(2*0)+(1*9)=93
93 % 10 = 3
So 102565-09-3 is a valid CAS Registry Number.

102565-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-N-(2-phenyl-2-thiophen-2-ylethenyl)-5-(trifluoromethyl)-1-benzothiophene-2-carboxamide

1.2 Other means of identification

Product number -
Other names N-[2-phenyl-2-(2-thienyl)]ethenyl-3-hydroxy-5-trifluoromethylbenzo[b]thiophene-2-carboxamide

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:102565-09-3 SDS

102565-09-3Relevant articles and documents

Stereoselective disposition of the geometric isomers of a novel lipoxygenase cyclo-oxygenase inhibitor in dog and photochemical interconversion of its isomers

Matuszewski,Kanovsky,Constanzer,Yeh,Bayne

, p. 880 - 884 (1988)

A sensitive (10 ng/mL) and specific high-performance liquid chromatographic (HPLC) assay, with electrochemical (EC) detection, for the geometric isomers of 3-hydroxy-N-(2-phenyl-2-(2-thienyl)ethenyl-5-(trifluoromethyl)benzo(b thiophene-2-carboxamide in dog and human plasma has been developed. Both isomers strongly absorb light, leading to an efficient E ? Z photoisomerization. After iv administration of a single isomer (Z) to a dog, only the Z isomer was detected in plasma; no in vivo conversion to the E isomer was observed. However, when a mixture of the E and Z isomers (58.6:41.4) was administered in the same manner to the same dog, the E:Z ratio decreased significantly to 47.5:52.5 six hours after drug administration, indicating stereoselective disposition of the isomers. The elimination of the E isomer was found to be faster than that of the Z isomer.

N-ALKENYL-3-HYDROXYBENZO[B]THIOPHENE-2-CARBOXAMIDE DERIVATIVES AS DUAL CYCLOOXYGENASE AND LIPOXYGENASE INHIBITORS

-

, (2008/06/13)

Method for increasing resistance to gastro-intestinal irritation, and for the treatment of pain, fever, inflammation, arthritic conditions, asthma, allergic disorders, skin diseases, cardiovascular disorders, psoriasis, inflammatory bowel disease, glaucom

N-alkenyl-3-hydroxybenzo[b]thiophene-2-carboxamide derivatives as dual cyclooxygenase and lipoxygenase inhibitors

-

, (2008/06/13)

N-Alkenyl-3-hydroxybenzo[b]thiophene-2-carboxamide derivatives have been prepared by: (1) treating a substituted 2-halobenzoate with thioacetamide followed by N-alkenylation with appropriate agents, such as aldehydes, ketones, enol ethers, epoxides, aceta

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