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4-ETHYL-5-(4-METHOXYPHENYL)-4H-1,2,4-TRIAZOLE-3-THIOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 168968-58-9 Structure
  • Basic information

    1. Product Name: 4-ETHYL-5-(4-METHOXYPHENYL)-4H-1,2,4-TRIAZOLE-3-THIOL
    2. Synonyms: ASISCHEM Y67820;AKOS BBS-00003324;4-ETHYL-5-(4-METHOXYPHENYL)-4H-1,2,4-TRIAZOLE-3-THIOL;TIMTEC-BB SBB009883
    3. CAS NO:168968-58-9
    4. Molecular Formula: C11H13N3OS
    5. Molecular Weight: 235.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 168968-58-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-ETHYL-5-(4-METHOXYPHENYL)-4H-1,2,4-TRIAZOLE-3-THIOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-ETHYL-5-(4-METHOXYPHENYL)-4H-1,2,4-TRIAZOLE-3-THIOL(168968-58-9)
    11. EPA Substance Registry System: 4-ETHYL-5-(4-METHOXYPHENYL)-4H-1,2,4-TRIAZOLE-3-THIOL(168968-58-9)
  • Safety Data

    1. Hazard Codes: Xi,Xn
    2. Statements: 22
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 168968-58-9(Hazardous Substances Data)

168968-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 168968-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,9,6 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 168968-58:
(8*1)+(7*6)+(6*8)+(5*9)+(4*6)+(3*8)+(2*5)+(1*8)=209
209 % 10 = 9
So 168968-58-9 is a valid CAS Registry Number.

168968-58-9Downstream Products

168968-58-9Relevant articles and documents

Design, synthesis and molecular docking of new N-4-piperazinyl ciprofloxacin-triazole hybrids with potential antimicrobial activity

Mohammed, Hamada H.H.,Abdelhafez, El-Shimaa M.N.,Abbas, Samar H.,Moustafa, Gamal A.I.,Hauk, Glenn,Berger, James M.,Mitarai, Satoshi,Arai, Masayoshi,Abd El-Baky, Rehab M.,Abuo-Rahma, Gamal El-Din A.

, (2019/05/01)

New N-4-piperazinyl ciprofloxacin-triazole hybrids 6a-o were prepared and characterized. The in vitro antimycobacterial activity revealed that compound 6a experienced promising antimycobacterial activity against Mycobactrium smegmatis compared with the reference isoniazide (INH). Additionally, compound 6a exhibited broad spectrum antibacterial activity against all the tested strains either Gram-positive or Gram-negative bacteria compared with the reference ciprofloxacin. Also, compounds 6g and 6i displayed considerable antifungal activity compared with the reference ketoconazole. DNA cleavage assay of the highly active compounds 6c and 6h showed a good correlation between the Mycobactrium cleaved DNA gyrase assay and their in vitro antimycobactrial activity. Moreover, molecular modeling studies were done for the designed ciprofloxacin derivatives to predict their binding modes towards Topoisomerase II enzyme (PDB: 5bs8).

Cytoprotection utilizing aryltriazol-3-thiones

-

, (2008/06/13)

5-Aryltriazol-3-thiones are useful for inhibiting adhesion of Mac-1 and thereby providing cytoprotection for diseases mediated by Mac-1 adhesion.

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