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  • 63868-09-7 Structure
  • Basic information

    1. Product Name: MCL-115
    2. Synonyms: MCL-115
    3. CAS NO:63868-09-7
    4. Molecular Formula:
    5. Molecular Weight: 375.511
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63868-09-7.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: MCL-115(CAS DataBase Reference)
    10. NIST Chemistry Reference: MCL-115(63868-09-7)
    11. EPA Substance Registry System: MCL-115(63868-09-7)
  • 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: 63868-09-7(Hazardous Substances Data)

63868-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63868-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,6 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63868-09:
(7*6)+(6*3)+(5*8)+(4*6)+(3*8)+(2*0)+(1*9)=157
157 % 10 = 7
So 63868-09-7 is a valid CAS Registry Number.

63868-09-7Downstream Products

63868-09-7Relevant articles and documents

Mixed κ agonists and μ agonists/antagonists as potential pharmacotherapeutics for cocaine abuse: Synthesis and opioid receptor binding affinity of N-substituted derivatives of morphinan

Neumeyer, John L,Gu, Xiao-Hui,Van Vliet,DeNunzio, Nicholas J,Rusovici, Daniela E,Cohen, Dana J,Negus,Mello, Nancy K,Bidlack, Jean M

, p. 2735 - 2740 (2001)

A series of new N-substituted derivatives of morphinan was synthesized and their binding affinity for the three opioid receptors (μ, δ, and κ) was determined. A paradoxical effect of N-propargyl (MCL-117) and N-(3-iodoprop-(2E)-enyl) (MCL-118) substituents on the binding affinities for the μ and κ opioid receptors was observed. All of these novel derivatives showed a preference for the μ and κ versus δ binding.

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