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Piperazine, 1-(1-methylethyl)-4-[(4-nitrophenyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 519006-12-3 Structure
  • Basic information

    1. Product Name: Piperazine, 1-(1-methylethyl)-4-[(4-nitrophenyl)sulfonyl]-
    2. Synonyms: Piperazine, 1-(1-methylethyl)-4-[(4-nitrophenyl)sulfonyl]-;1-[(4-nitrophenyl)sulfonyl]-4-(propan-2-yl)piperazine
    3. CAS NO:519006-12-3
    4. Molecular Formula: C13H19N3O4S
    5. Molecular Weight: 313.37266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 519006-12-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Piperazine, 1-(1-methylethyl)-4-[(4-nitrophenyl)sulfonyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Piperazine, 1-(1-methylethyl)-4-[(4-nitrophenyl)sulfonyl]-(519006-12-3)
    11. EPA Substance Registry System: Piperazine, 1-(1-methylethyl)-4-[(4-nitrophenyl)sulfonyl]-(519006-12-3)
  • 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: 519006-12-3(Hazardous Substances Data)

519006-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 519006-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,9,0,0 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 519006-12:
(8*5)+(7*1)+(6*9)+(5*0)+(4*0)+(3*6)+(2*1)+(1*2)=123
123 % 10 = 3
So 519006-12-3 is a valid CAS Registry Number.

519006-12-3Relevant articles and documents

Identification of N-phenyl-3-methoxy-4-pyridinones as orally bioavailable H3 receptor antagonists and β-amyloid aggregation inhibitors for the treatment of Alzheimer's disease

Zhang, Minkui,Tang, Li,Jiang, Liu,Wei, Jun,Hu, Yongzhou,Sheng, Rong

, (2021/01/06)

Based on our previous work, a series of N-phenyl-3-methoxy-4-pyridinone derivatives were designed as orally bioavailable dual functional agents for therapy of Alzheimer's disease, through introducing alkyloxy moiety into 4-pyridinone ring to avoid the pos

Exploration of secondary and tertiary pharmacophores in unsymmetrical N,N′-diaryl urea inhibitors of soluble epoxide hydrolase

Anandan, Sampath-Kumar,Gless, Richard D.

scheme or table, p. 2740 - 2744 (2010/07/15)

The impact of various secondary and tertiary pharmacophores on in vitro potency of soluble epoxide hydrolase (sEH) inhibitors based on the unsymmetrical urea scaffold 1 is discussed. N,N′-Diaryl urea inhibitors of soluble epoxide hydrolase exhibit subtle variations in inhibitory potency depending on the secondary pharmacophore but tolerate considerable structural variation in the second linker/tertiary pharmacophore fragment.

SOLUBLE EPOXIDE HYDROLASE INHIBITORS

-

Page/Page column 53-54, (2008/06/13)

Disclosed are sulfonamide compounds and compositions that inhibit soluble epoxide hydrolase (sEH), methods for preparing the compounds and compositions, and methods for treating patients with such compounds and compositions. The compounds, compositions, and methods are useful for treating a variety of sEH mediated diseases, including hypertensive, cardiovascular, inflammatory, pulmonary, and diabetes-related diseases.

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