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  • 214326-05-3 Structure
  • Basic information

    1. Product Name: C26H30FNO3
    2. Synonyms: C26H30FNO3
    3. CAS NO:214326-05-3
    4. Molecular Formula:
    5. Molecular Weight: 423.528
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 214326-05-3.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: C26H30FNO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C26H30FNO3(214326-05-3)
    11. EPA Substance Registry System: C26H30FNO3(214326-05-3)
  • 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: 214326-05-3(Hazardous Substances Data)

214326-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214326-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,3,2 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 214326-05:
(8*2)+(7*1)+(6*4)+(5*3)+(4*2)+(3*6)+(2*0)+(1*5)=93
93 % 10 = 3
So 214326-05-3 is a valid CAS Registry Number.

214326-05-3Downstream Products

214326-05-3Relevant articles and documents

Synthesis and preliminary biological evaluation of new α-amino amide anticonvulsants incorporating a dextromethorphan moiety

Pevarello, Paolo,Traquandi, Gabriella,Bonsignori, Alberto,McArthur, Robert A.,Maj, Roberto,Caccia, Carla,Salvati, Patricia,Varasi, Mario

, p. 1783 - 1788 (2007/10/03)

Dextromethorphan 1 is an effective neuroprotectant in animal models of epilepsy and ischemia but showed side-effects during clinical trials limiting its potential use in a clinical setting. Here we describe the enantioselective and enantiospecific syntheses and the initial in vitro and in vivo biological evaluation of new hybrid structures between 1 and a previously disclosed α-amino amide anticonvulsant (3).

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