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  • 1429124-22-0 Structure
  • Basic information

    1. Product Name: C18H22ClN5
    2. Synonyms: C18H22ClN5
    3. CAS NO:1429124-22-0
    4. Molecular Formula:
    5. Molecular Weight: 343.859
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1429124-22-0.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: C18H22ClN5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H22ClN5(1429124-22-0)
    11. EPA Substance Registry System: C18H22ClN5(1429124-22-0)
  • 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: 1429124-22-0(Hazardous Substances Data)

1429124-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1429124-22-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,1,2 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1429124-22:
(9*1)+(8*4)+(7*2)+(6*9)+(5*1)+(4*2)+(3*4)+(2*2)+(1*2)=140
140 % 10 = 0
So 1429124-22-0 is a valid CAS Registry Number.

1429124-22-0Upstream product

1429124-22-0Downstream Products

1429124-22-0Relevant articles and documents

Synthesis and antimicrobial activity of polyhalo isophthalonitrile derivatives

Huang, Chao,Yan, Sheng-Jiao,He, Neng-Qin,Tang, Ya-Juan,Wang, Xing-Hong,Lin, Jun

, p. 2399 - 2403 (2013)

A series of polyhalo isophthalonitrile derivatives (3 and 4) that incorporate a variety of substituents at the 2-, 4-, 5- and/or 6-positions of the isophthalonitrile moieties have been designed and synthesized. These derivatives were evaluated for their antimicrobial activity against Staphylococcus aureus, Bacillus cereus (Gram-positive bacteria), Escherichia coli, Pseudomonas aeruginosa (Gram-negative bacteria); and Candida albicans (Fungi). Compounds 3 and 4 showed stronger inhibition of Gram-positive bacteria and fungi growth, and the antimicrobial ability of compound 3j (a 4-(benzylamino)-5-chloro-2,6-difluoro analog, MIC[SA] = 0.5 μg/mL; MIC[BC] = 0.4 μg/mL; MIC[CA] = 0.5 μg/mL) were close to nofloxacin and fluconazole and identified as the most potent antimicrobial agents in the series. The preliminary analysis of structure-activity relationships is also discussed.

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