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N-allyl-N-(1,4-dioxaspiro<5.4>deca-7-en-8-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 221216-05-3 Structure
  • Basic information

    1. Product Name: N-allyl-N-(1,4-dioxaspiro<5.4>deca-7-en-8-yl)benzamide
    2. Synonyms:
    3. CAS NO:221216-05-3
    4. Molecular Formula:
    5. Molecular Weight: 299.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 221216-05-3.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: N-allyl-N-(1,4-dioxaspiro<5.4>deca-7-en-8-yl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-allyl-N-(1,4-dioxaspiro<5.4>deca-7-en-8-yl)benzamide(221216-05-3)
    11. EPA Substance Registry System: N-allyl-N-(1,4-dioxaspiro<5.4>deca-7-en-8-yl)benzamide(221216-05-3)
  • 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: 221216-05-3(Hazardous Substances Data)

221216-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221216-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,2,1 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 221216-05:
(8*2)+(7*2)+(6*1)+(5*2)+(4*1)+(3*6)+(2*0)+(1*5)=73
73 % 10 = 3
So 221216-05-3 is a valid CAS Registry Number.

221216-05-3Downstream Products

221216-05-3Relevant articles and documents

Synthesis and dopaminergic properties of benzo-fused analogues of quinpirole and quinelorane

Doll, Martin K.-H.,Nichols, David E.,Kilts, Jason D.,Prioleau, Cassandra,Lawler, Cindy P.,Lewis, Mechelle M.,Mailman, Richard B.

, p. 935 - 940 (1999)

In an analogy to the potent catechol dopamine D1 agonists dihydrexidine (1) and dinapsoline (2), benzo rings were fused onto the structures of the dopamine D2-selective agonists quinelorane (3) and quinpirole (4). Each of the phenyl

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