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CAS

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327031-10-7

4-(2-hydroxy-3,5-dibromobenzylideneamino)-3-phenyl-1,2,4-triazole-5-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 327031-10-7 Structure

  • Basic information

    1. Product Name: 4-(2-hydroxy-3,5-dibromobenzylideneamino)-3-phenyl-1,2,4-triazole-5-thione
    2. Synonyms: 4-(2-hydroxy-3,5-dibromobenzylideneamino)-3-phenyl-1,2,4-triazole-5-thione
    3. CAS NO:327031-10-7
    4. Molecular Formula:
    5. Molecular Weight: 454.145
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 327031-10-7.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: 4-(2-hydroxy-3,5-dibromobenzylideneamino)-3-phenyl-1,2,4-triazole-5-thione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(2-hydroxy-3,5-dibromobenzylideneamino)-3-phenyl-1,2,4-triazole-5-thione(327031-10-7)
    11. EPA Substance Registry System: 4-(2-hydroxy-3,5-dibromobenzylideneamino)-3-phenyl-1,2,4-triazole-5-thione(327031-10-7)

  • 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: 327031-10-7(Hazardous Substances Data)

327031-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 327031-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,7,0,3 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 327031-10:
(8*3)+(7*2)+(6*7)+(5*0)+(4*3)+(3*1)+(2*1)+(1*0)=97
97 % 10 = 7
So 327031-10-7 is a valid CAS Registry Number.

327031-10-7Downstream Products

327031-10-7Relevant articles and documents

Efficient synthesis and antimicrobial activity of some novel S-β-d-glucosides of 5-aryl-1,2,4-triazole-3-thiones derivatives

Ji, Dan,Lu, Junrui,Lu, Bowei,Xin, Chunwei,Mu, Jiangbei,Li, Jianfa,Peng, Chunyong,Bao, Xiurong

, p. 1997 - 2000 (2013/04/23)

A series of 3-S-β-d-glucosides-4-arylideneamino-5-aryl-1,2,4-triazoles were rationally designed and synthesized according to the principle of superposition of bioactive substructures by the combination of 1,2,4-triazole, Schiff base and glucosides. The structures of the target compounds have been characterized by 1H NMR, 13C NMR, IR, MS and HRMS. All the newly synthesized compounds have been evaluated for their antimicrobial activities in vitro against Staphylococcus aureus (ATCC 6538), Escherichia coli (ATCC 8099) as well as Monilia albican (ATCC 10231). The bioactive assay showed that most of the tested compounds displayed variable inhibitory effects on the growth of the Gram-positive bacterial strain (Staphylococcus aureus), Gram-negative bacterial strains (Escherichia coli) and fungal strains (Monilia albican). All the target compounds exhibited better antifungal activity than antibacterial activity. Especially, compounds 6b, 6c, 6f, 6j, 6k and 6l showed excellent activity against fungus Monilia albican with MIC values of 16 μg/mL.

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