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C22H16N4O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1264954-04-2 Structure
  • Basic information

    1. Product Name: C22H16N4O
    2. Synonyms: C22H16N4O
    3. CAS NO:1264954-04-2
    4. Molecular Formula:
    5. Molecular Weight: 352.395
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1264954-04-2.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: C22H16N4O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H16N4O(1264954-04-2)
    11. EPA Substance Registry System: C22H16N4O(1264954-04-2)
  • 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: 1264954-04-2(Hazardous Substances Data)

1264954-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1264954-04-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,4,9,5 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1264954-04:
(9*1)+(8*2)+(7*6)+(6*4)+(5*9)+(4*5)+(3*4)+(2*0)+(1*4)=172
172 % 10 = 2
So 1264954-04-2 is a valid CAS Registry Number.

1264954-04-2Downstream Products

1264954-04-2Relevant articles and documents

Antifungal agents. Part 4: Synthesis and antifungal activities of novel indole[1,2-c]-1,2,4-benzotriazine derivatives against phytopathogenic fungi in vitro

Xu, Hui,Fan, Ling-Ling

, p. 364 - 369 (2011/03/17)

A series of novel indole[1,2-c]-1,2,4-benzotriazine derivatives were obtained by a modified Sandmeyer reaction in the presence of tert-butylnitrite (t-BuONO). As compared with hymexazol, a commercially available agricultural fungicide, at the concentration of 50 μg/mL, two indole[1,2-c]-1,2,4- benzotriazines, 5h and 5k, exhibited the more promising and pronounced antifungal activities in vitro against five phytopathogenic fungi. It clearly demonstrated that introduction of appropriate substituents on the indolyl ring of indole[1,2-c]-1,2,4-benzotriazine (5a) would lead to the more potent derivatives.

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