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1H-Benzimidazol-2-amine, 1-phenyl-5-(1-piperidinylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 509093-76-9 Structure
  • Basic information

    1. Product Name: 1H-Benzimidazol-2-amine, 1-phenyl-5-(1-piperidinylmethyl)-
    2. Synonyms:
    3. CAS NO:509093-76-9
    4. Molecular Formula: C19H22N4
    5. Molecular Weight: 306.41
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 509093-76-9.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: 1H-Benzimidazol-2-amine, 1-phenyl-5-(1-piperidinylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Benzimidazol-2-amine, 1-phenyl-5-(1-piperidinylmethyl)-(509093-76-9)
    11. EPA Substance Registry System: 1H-Benzimidazol-2-amine, 1-phenyl-5-(1-piperidinylmethyl)-(509093-76-9)
  • 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: 509093-76-9(Hazardous Substances Data)

509093-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 509093-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,9,0,9 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 509093-76:
(8*5)+(7*0)+(6*9)+(5*0)+(4*9)+(3*3)+(2*7)+(1*6)=159
159 % 10 = 9
So 509093-76-9 is a valid CAS Registry Number.

509093-76-9Relevant articles and documents

Discovery of potent, selective, and orally bioavailable inhibitors of interleukin-1 receptor-associate kinase-4

Wang, Zhulun,Sun, Daqing,Johnstone, Sheree,Cao, Zhaodan,Gao, Xiong,Jaen, Juan C.,Liu, Jingqian,Lively, Sarah,Miao, Shichang,Sudom, Athena,Tomooka, Craig,Walker, Nigel P.C.,Wright, Matthew,Yan, Xuelei,Ye, Qiuping,Powers, Jay P.

, p. 5546 - 5550 (2015/11/17)

In this Letter, we report the continued optimization of the N-acyl-2-aminobenzimidazole series, focusing in particular on the N-alkyl substituent and 5-position of the benzimidazole based on the binding mode and the early SAR. These efforts led to the discovery of 16, a highly potent, selective, and orally bioavailable inhibitor of IRAK-4.

Benzimidazole derivatives

-

, (2008/06/13)

Compounds, pharmaceutical compositions and methods are provided that are useful in the treatment of inflammatory and immune-related conditions or disorders. In particular, the invention provides compounds which modulate the expression and/or function of proteins involved in inflammation, immune response regulation and cell proliferation. The subject compounds are 2-amino-imidazole derivatives.

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