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1304778-15-1

TC-F 2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1304778-15-1 Structure

  • Basic information

    1. Product Name: TC-F 2
    2. Synonyms: TC-F 2
    3. CAS NO:1304778-15-1
    4. Molecular Formula: C26H25N5O2
    5. Molecular Weight: 439.509
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1304778-15-1.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: TC-F 2(CAS DataBase Reference)
    10. NIST Chemistry Reference: TC-F 2(1304778-15-1)
    11. EPA Substance Registry System: TC-F 2(1304778-15-1)

  • 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: 1304778-15-1(Hazardous Substances Data)

1304778-15-1 Usage

Uses

TC-F 2 is a potent, noncovalent fatty acid amide hydrolase (FAAH) inhibitor.

Check Digit Verification of cas no

The CAS Registry Mumber 1304778-15-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,7,7 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1304778-15:
(9*1)+(8*3)+(7*0)+(6*4)+(5*7)+(4*7)+(3*8)+(2*1)+(1*5)=151
151 % 10 = 1
So 1304778-15-1 is a valid CAS Registry Number.

1304778-15-1Downstream Products

1304778-15-1Relevant articles and documents

Identification of potent, noncovalent fatty acid amide hydrolase (FAAH) inhibitors

Gustin, Darin J.,Ma, Zhihua,Min, Xiaoshan,Li, Yihong,Hedberg, Christine,Guimaraes, Cris,Porter, Amy C.,Lindstrom, Michelle,Lester-Zeiner, Dianna,Xu, Guifen,Carlson, Timothy J.,Xiao, Shouhua,Meleza, Cesar,Connors, Richard,Wang, Zhulun,Kayser, Frank

, p. 2492 - 2496 (2011/05/15)

Starting from a series of ureas that were determined to be mechanism-based inhibitors of FAAH, several spirocyclic ureas and lactams were designed and synthesized. These efforts identified a series of novel, noncovalent FAAH inhibitors with in vitro potency comparable to known covalent FAAH inhibitors. The mechanism of action for these compounds was determined through a combination of SAR and co-crystallography with rat FAAH.

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