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rac-2-amino-N-[(4-chlorophenyl)phenylmethyl]acetamide hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1009371-01-0 Structure
  • Basic information

    1. Product Name: rac-2-amino-N-[(4-chlorophenyl)phenylmethyl]acetamide hydrochloride
    2. Synonyms: rac-2-amino-N-[(4-chlorophenyl)phenylmethyl]acetamide hydrochloride
    3. CAS NO:1009371-01-0
    4. Molecular Formula:
    5. Molecular Weight: 311.211
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1009371-01-0.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: rac-2-amino-N-[(4-chlorophenyl)phenylmethyl]acetamide hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: rac-2-amino-N-[(4-chlorophenyl)phenylmethyl]acetamide hydrochloride(1009371-01-0)
    11. EPA Substance Registry System: rac-2-amino-N-[(4-chlorophenyl)phenylmethyl]acetamide hydrochloride(1009371-01-0)
  • 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: 1009371-01-0(Hazardous Substances Data)

1009371-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1009371-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,9,3,7 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1009371-01:
(9*1)+(8*0)+(7*0)+(6*9)+(5*3)+(4*7)+(3*1)+(2*0)+(1*1)=110
110 % 10 = 0
So 1009371-01-0 is a valid CAS Registry Number.

1009371-01-0Relevant articles and documents

Design, synthesis and structure-activity relationship of simple bis-amides as potent inhibitors of GlyT1

Jolidon, Synese,Alberati, Daniela,Dowle, Adam,Fischer, Holger,Hainzl, Dominik,Narquizian, Robert,Norcross, Roger,Pinard, Emmanuel

scheme or table, p. 5533 - 5536 (2009/06/18)

Several novel classes of potent and small amide-type inhibitors of glycine transport (GlyT1) were developed through sequential simplification of a benzodiazepinone-lead structure identified from a high-throughput screening. The most potent compounds of these structurally simple classes show low nanomolar inhibition at the GlyT1 target.

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