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  • 1620883-56-8 Structure
  • Basic information

    1. Product Name: C14H17N3O2
    2. Synonyms: C14H17N3O2
    3. CAS NO:1620883-56-8
    4. Molecular Formula:
    5. Molecular Weight: 259.308
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1620883-56-8.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: C14H17N3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H17N3O2(1620883-56-8)
    11. EPA Substance Registry System: C14H17N3O2(1620883-56-8)
  • 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: 1620883-56-8(Hazardous Substances Data)

1620883-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1620883-56-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,8,8 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1620883-56:
(9*1)+(8*6)+(7*2)+(6*0)+(5*8)+(4*8)+(3*3)+(2*5)+(1*6)=168
168 % 10 = 8
So 1620883-56-8 is a valid CAS Registry Number.

1620883-56-8Downstream Products

1620883-56-8Relevant articles and documents

Synthesis and bioactivities of novel pyrazole oxime derivatives containing a 5-trifluoromethylpyridyl moiety

Dai, Hong,Chen, Jia,Li, Hong,Dai, Baojiang,He, Haibing,Fang, Yuan,Shi, Yujun

, (2016)

In this study, in order to find novel biologically active pyrazole oxime compounds, a series of pyrazole oxime derivatives containing a 5-trifluoromethylpyridyl moiety were synthesized. Preliminary bioassays indicated that most title compounds were found to display good to excellent acaricidal activity against Tetranychus cinnabarinus at a concentration of 200 μg/mL, and some designed compounds still showed excellent acaricidal activity against Tetranychus cinnabarinus at the concentration of 10 μg/mL, especially since the inhibition rates of compounds 8e, 8f, 8l, 8m, 8n, 8p, and 8q were all 100.00%. Interestingly, some target compounds exhibited moderate to good insecticidal activities against Plutella xylostella and Aphis craccivora at a concentration of 200 μg/mL; furthermore, compounds 8e and 8l possessed outstanding insecticidal activities against Plutella xylostella under the concentration of 50 μg/mL.

The thiazoylmethoxy modification on pyrazole oximes: Synthesis and insecticidal biological evaluation beyond acaricidal activity

Dai, Hong,Xiao, Yan-Shuang,Li, Zhong,Xu, Xiao-Yong,Qian, Xu-Hong

, p. 1014 - 1016 (2014/08/18)

A series of new pyrazole oximes bearing substituted thiazole ring were designed and prepared. The structures of the title compounds were identified by spectral analyses. The results of primary bioassay indicated that some targeted compounds exhibited promising insecticidal activity besides acaricidal activity, particularly; compounds 8c and 8d were more potent against Tetranychus cinnabarinus and Plutella xylostella than other analogues.

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