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C16H20N2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1338816-22-0 Structure
  • Basic information

    1. Product Name: C16H20N2O
    2. Synonyms:
    3. CAS NO:1338816-22-0
    4. Molecular Formula:
    5. Molecular Weight: 256.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1338816-22-0.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: C16H20N2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H20N2O(1338816-22-0)
    11. EPA Substance Registry System: C16H20N2O(1338816-22-0)
  • 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: 1338816-22-0(Hazardous Substances Data)

1338816-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338816-22-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,8,1 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1338816-22:
(9*1)+(8*3)+(7*3)+(6*8)+(5*8)+(4*1)+(3*6)+(2*2)+(1*2)=170
170 % 10 = 0
So 1338816-22-0 is a valid CAS Registry Number.

1338816-22-0Downstream Products

1338816-22-0Relevant articles and documents

Acylglycinamides as inhibitors of glycine transporter type 1

Blunt, Richard,Porter, Roderick,Johns, Amanda,Nash, David,Puckey, Gemma,Wyman, Paul,Herdon, Hugh,Teague, Simon,Hadden, Victoria,Fontana, Stefano,Gordon, Laurie

scheme or table, p. 6176 - 6179 (2011/10/18)

A screening hit was used as the basis for the core structure of a new series of acylglycinamide GlyT-1 inhibitors. Investigation of the SAR around four areas of diversity used facile chemistry to prepare compounds quickly. By focussing on reducing the lipophilicity and improving the aqueous solubility in the series we were able to prepare a compound (17e) with a good level of activity at GlyT-1, selectivity over GlyT-2 and moderate oral bioavailability.

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