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  • 1200835-89-7 Structure
  • Basic information

    1. Product Name: C11H15N5O2
    2. Synonyms: C11H15N5O2
    3. CAS NO:1200835-89-7
    4. Molecular Formula:
    5. Molecular Weight: 249.272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1200835-89-7.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: C11H15N5O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H15N5O2(1200835-89-7)
    11. EPA Substance Registry System: C11H15N5O2(1200835-89-7)
  • 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: 1200835-89-7(Hazardous Substances Data)

1200835-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1200835-89-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,0,8,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1200835-89:
(9*1)+(8*2)+(7*0)+(6*0)+(5*8)+(4*3)+(3*5)+(2*8)+(1*9)=117
117 % 10 = 7
So 1200835-89-7 is a valid CAS Registry Number.

1200835-89-7Relevant articles and documents

Synthesis, insecticidal activities, and molecular docking studies of 1,5-disubstituted-1,3,5-hexahydrotriazine-2-(N-nitro)imines

Sun, Chuan-Wen,Wang, Hai-Feng,Zhu, Jun,Yang, Ding-Rong,Jin, Jia,Xing, Jia-Hua

experimental part, p. 829 - 835 (2011/09/16)

Figure represented. A series of novel neonicotinoids analogs were designed by modifying the pharmacophore of imidacloprid to 1,3,5-hexahydrotriazine conjugated to nitroimine (iNNO2) and introducing the phenyl or arylmethyl at the 5-position, and their insecticidal activities were evaluated. Introducing a heterocyclic methyl at 5-position increased the insecticidal activities, whereas other phenyl, phenylmethyl or phenylethyl substituents were unfavorable to activities. Molecular docking study was also performed to clarify the interactions of the most potent analog 1-((6-chloropyridin-3-yl)methyl)-5- (3-pyridylmethyl)-1,3,5-hexahydrotriazine-2-(N-nitro) imine (7s) with the target nicotinic acetylcholine receptor, which explained the structure-activity relationships observed in vitro, and revealed further possibilities for insecticide development.

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