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107943-86-2

3-(3-chlorophenyl)-2-(3-chlorophenylimino)thiazolidin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107943-86-2 Structure

  • Basic information

    1. Product Name: 3-(3-chlorophenyl)-2-(3-chlorophenylimino)thiazolidin-4-one
    2. Synonyms:
    3. CAS NO:107943-86-2
    4. Molecular Formula:
    5. Molecular Weight: 337.229
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107943-86-2.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: 3-(3-chlorophenyl)-2-(3-chlorophenylimino)thiazolidin-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3-chlorophenyl)-2-(3-chlorophenylimino)thiazolidin-4-one(107943-86-2)
    11. EPA Substance Registry System: 3-(3-chlorophenyl)-2-(3-chlorophenylimino)thiazolidin-4-one(107943-86-2)

  • 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: 107943-86-2(Hazardous Substances Data)

107943-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107943-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,4 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107943-86:
(8*1)+(7*0)+(6*7)+(5*9)+(4*4)+(3*3)+(2*8)+(1*6)=142
142 % 10 = 2
So 107943-86-2 is a valid CAS Registry Number.

107943-86-2Relevant articles and documents

Novel non-peptidic small molecule inhibitors of secreted aspartic protease 2 (SAP2) for the treatment of resistant fungal infections

Dong, Guoqiang,Liu, Yang,Wu, Ying,Tu, Jie,Chen, Shuqiang,Liu, Na,Sheng, Chunquan

supporting information, p. 13535 - 13538 (2019/01/05)

Targeting secreted aspartic protease 2 (SAP2), a kind of virulence factor, represents a new strategy for antifungal drug discovery. In this report, the first-generation of small molecule SAP2 inhibitors was rationally designed and optimized using a structure-based approach. In particular, inhibitor 23h was highly potent and selective and showed good antifungal potency for the treatment of resistant Candida albicans infections.

Synthesis of novel 4-thiazolidione derivatives as antibacterial agents against drug-resistant Staphylococcus epidermidis

Zhao, Dan,Liu, Huayong,Zheng, Likang,He, Guozhen,Qu, Di,Han, Shiqing

, p. 3743 - 3750 (2013/07/26)

A series of novel substituted 4-thiazolidione derivatives were designed, synthesized, and evaluated in vitro for their antibacterial activities, in comparison with methicillin and ampicillin. Compounds (7d, 7h-k) exhibit good potency in inhibiting the growth of Staphylococcus epidermidis (MIC: 1.57-3.13 μM). Further antibacterial effects of compounds (7d, 7h-k) were investigated using clinical isolates (methicillin-resistant Staphylococcus epidermidis and methicillin-resistant Staphylococcus aureus), in comparison with methicillin and levofloxacin. Compound 7k showed the most potent antibacterial activities among the synthesized compounds.

Synthesis and biological evaluation of halogenated 2-arylimino-3- arythiazolidine-4-ones containing benzoic acid fragments as antibacterial agents

Zhang, Jie,Zheng, Likang,Liu, Huayong,Zhao, Dan,Qu, Di,Han, Shiqing

, p. 928 - 934 (2013/12/04)

A series of halogenated 2-arylimino-3-ary-thiazolidine-4-ones containing (5-furan-2-yl)-benzoic acid or (5-thiophene-2-yl)-benzoic acid fragments was synthesized, and evaluated in vitro for their antibacterial activity, antibiofilm activity, erythrocyte h

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