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1446419-04-0

C15H19N3O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446419-04-0 Structure

  • Basic information

    1. Product Name: C15H19N3O4
    2. Synonyms:
    3. CAS NO:1446419-04-0
    4. Molecular Formula:
    5. Molecular Weight: 305.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446419-04-0.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: C15H19N3O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H19N3O4(1446419-04-0)
    11. EPA Substance Registry System: C15H19N3O4(1446419-04-0)

  • 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: 1446419-04-0(Hazardous Substances Data)

1446419-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446419-04-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,4,1 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1446419-04:
(9*1)+(8*4)+(7*4)+(6*6)+(5*4)+(4*1)+(3*9)+(2*0)+(1*4)=160
160 % 10 = 0
So 1446419-04-0 is a valid CAS Registry Number.

1446419-04-0Downstream Products

1446419-04-0Relevant articles and documents

Synthesis and acrosin inhibitory activities of 5-phenyl-1H-pyrazole-3- carboxylic acid amide derivatives

Tian, Wei,Han, Guangqian,Zhu, Ju,Qi, Jingjing,Chen, Qianqian,Zhao, Juntao,Zheng, Canhui,Zhang, Ling,Zhou, Youjun,Lv, Jiaguo

, p. 4177 - 4184 (2013/07/25)

A series of novel 5-phenyl-1H-pyrazole-3-carboxylic acid amide derivatives were designed, synthesized, and their acrosin inhibitory activities in vitro were evaluated. The results of the acrosin inhibitory activity showed that all target compounds were mo

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