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2069-49-0

1-(5-chlorothiophen-2-yl)-3-(4-fluorophenyl)prop-2-en-1-one is a complex organic chemical compound characterized by a unique molecular structure. It consists of a prop-2-en-1-one backbone, which is a three-carbon chain with a carbonyl group at one end and a double bond at the other. The molecule features a 5-chlorothiophen-2-yl group attached to the first carbon of the prop-2-en-1-one chain, which introduces a chlorine atom and a thiophene ring into the structure. Additionally, a 4-fluorophenyl group is attached to the third carbon, contributing a fluorine atom and a phenyl ring to the molecule. 1-(5-chlorothiophen-2-yl)-3-(4-fluorophenyl)prop-2-en-1-one is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, due to its diverse functional groups and structural features.

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  • 2069-49-0 Structure

  • Basic information

    1. Product Name: 1-(5-chlorothiophen-2-yl)-3-(4-fluorophenyl)prop-2-en-1-one
    2. Synonyms: 1-(5-chlorothiophen-2-yl)-3-(4-fluorophenyl)prop-2-en-1-one
    3. CAS NO:2069-49-0
    4. Molecular Formula:
    5. Molecular Weight: 266.723
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2069-49-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(5-chlorothiophen-2-yl)-3-(4-fluorophenyl)prop-2-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(5-chlorothiophen-2-yl)-3-(4-fluorophenyl)prop-2-en-1-one(2069-49-0)
    11. EPA Substance Registry System: 1-(5-chlorothiophen-2-yl)-3-(4-fluorophenyl)prop-2-en-1-one(2069-49-0)

  • 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: 2069-49-0(Hazardous Substances Data)

2069-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2069-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2069-49:
(6*2)+(5*0)+(4*6)+(3*9)+(2*4)+(1*9)=80
80 % 10 = 0
So 2069-49-0 is a valid CAS Registry Number.

2069-49-0Downstream Products

2069-49-0Relevant articles and documents

A novel series of thiazolyl-pyrazoline derivatives: Synthesis and evaluation of antifungal activity, cytotoxicity and genotoxicity

Altintop, Mehlika Dilek,?demir, Ahmet,Turan-Zitouni, Gülhan,Ilgin, Sinem,Atli, ?zlem,Demirel, Rasime,Kaplancikli, Zafer Asim

, p. 342 - 352 (2015)

In the current work, new thiazolylepyrazoline derivatives (1e22) were synthesized and evaluated for their antifungal effects against pathogenic yeasts and molds using a broth microdilution assay. Ames assay was carried out to determine the genotoxicity of

An efficient synthesis of thiophene conjugated benzothiazepines: In vitro screening for their antimicrobial activity

RAGHAVENDRA,SUDEEP,KUMAR, K. AJAY,JAYADEVAPPA

, p. 2601 - 2605 (2020/10/22)

A series of novel thiophene conjugated benzothiazepines were synthesized by the reaction of chalcones with 2-aminobenzenethiol in citrus juice medium. The new compounds were characterized by spectroscopic studies. Results of in vitro antimicrobial evaluation of newly synthesized compounds 5a-j shows that the compounds 5a and 5c have excellent antimicrobial inhibition in the range of 12.5-25.0 μg/ mL against bacteria S. aureus, E. coli, P. aeruginosa and fungi A. niger, A. flavus organisms comparable to ciprofloxacin and nystatin and therefore these compounds might acts as lead molecules as antimicrobial agents.

Exploration of chlorinated thienyl chalcones: A new class of monoamine oxidase-B inhibitors

Mathew, Bijo,Haridas, Abitha,U?ar, Gülberk,Baysal, Ipek,Adeniyi, Adebayo A.,Soliman, Mahmoud E.S.,Joy, Monu,Mathew, Githa Elizabeth,Lakshmanan, Baskar,Jayaprakash, Venkatesan

, p. 680 - 695 (2016/07/06)

Chalcone has been reported to be a valid scaffold for the design of monoamine oxidase (MAO) inhibitors. This scenario has amplified the momentum for the discovery of heteroaryl based chalcone MAO inhibitors. In the present study, we have synthesized a ser

SOCl2 catalyzed cyclization of chalcones: Synthesis and spectral studies of some bio-potent 1H pyrazoles

Ranganathan, Kaliyaperumal,Suresh, Ramamoorthy,Vanangamudi, Ganesan,Thirumurthy, Kannan,Mayavel, Perumal,Thirunarayanan, Ganesamoorthy

, p. 271 - 288 (2014/06/24)

Some aryl-aryl 1H pyrazoles have been synthesised by cyclization of aryl chalcones and hydrazine hydrate in the presence of SOCl2. The yields of the pyrazoles are more than 85%. These pyrazoles are characterized by their physical con

Heteroaryl chalcones: Design, synthesis, X-ray crystal structures and biological evaluation

Chidan Kumar,Loh, Wan-Sin,Ooi, Chin Wei,Quah, Ching Kheng,Fun, Hoong-Kun

, p. 12707 - 12724 (2013/11/06)

Chalcone derivatives have attracted increasing attention due to their numerous pharmacological activities. Changes in their structures have displayed high degree of diversity that has proven to result in a broad spectrum of biological activities. The pres

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