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1-BOC-4-[2-AMINO-1-[2-(TRIFLUOROMETHYL)PHENYL]ETHYL]-PIPERAZINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 444892-52-8 Structure
  • Basic information

    1. Product Name: 1-BOC-4-[2-AMINO-1-[2-(TRIFLUOROMETHYL)PHENYL]ETHYL]-PIPERAZINE
    2. Synonyms: 1-BOC-4-[2-AMINO-1-[2-(TRIFLUOROMETHYL)PHENYL]ETHYL]-PIPERAZINE
    3. CAS NO:444892-52-8
    4. Molecular Formula: C18H26F3N3O2
    5. Molecular Weight: 373.416
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 444892-52-8.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: 1-BOC-4-[2-AMINO-1-[2-(TRIFLUOROMETHYL)PHENYL]ETHYL]-PIPERAZINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-BOC-4-[2-AMINO-1-[2-(TRIFLUOROMETHYL)PHENYL]ETHYL]-PIPERAZINE(444892-52-8)
    11. EPA Substance Registry System: 1-BOC-4-[2-AMINO-1-[2-(TRIFLUOROMETHYL)PHENYL]ETHYL]-PIPERAZINE(444892-52-8)
  • 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: 444892-52-8(Hazardous Substances Data)

444892-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 444892-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,8,9 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 444892-52:
(8*4)+(7*4)+(6*4)+(5*8)+(4*9)+(3*2)+(2*5)+(1*2)=178
178 % 10 = 8
So 444892-52-8 is a valid CAS Registry Number.

444892-52-8Relevant articles and documents

Privileged structure based ligands for melanocortin receptors - Substituted benzylic piperazine derivatives

Fisher, Matthew J.,Backer, Ryan T.,Collado, Ivan,De Frutos, Oscar,Husain, Saba,Hsiung, Hansen M.,Kuklish, Steve L.,Mateo, Ana I.,Mullaney, Jeffrey T.,Ornstein, Paul L.,Paredes, Cristina Garcia,O'Brian, Thomas P.,Richardson, Timothy I.,Shah, Jikesh,Zgombick, John M.,Briner, Karin

, p. 4973 - 4978 (2007/10/03)

Replacement of the aryl piperazine moiety in compound 1 with a variety of substituted benzylic piperazines (6) yields compounds that afford melanocortin receptor 4 (MCR4) activity. Analogs with ortho substitution on the aromatic ring afforded the highest

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