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1082113-82-3

C16H24N2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1082113-82-3 Structure

  • Basic information

    1. Product Name: C16H24N2O
    2. Synonyms: C16H24N2O
    3. CAS NO:1082113-82-3
    4. Molecular Formula:
    5. Molecular Weight: 260.379
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1082113-82-3.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: C16H24N2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H24N2O(1082113-82-3)
    11. EPA Substance Registry System: C16H24N2O(1082113-82-3)

  • 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: 1082113-82-3(Hazardous Substances Data)

1082113-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1082113-82-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,2,1,1 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1082113-82:
(9*1)+(8*0)+(7*8)+(6*2)+(5*1)+(4*1)+(3*3)+(2*8)+(1*2)=113
113 % 10 = 3
So 1082113-82-3 is a valid CAS Registry Number.

1082113-82-3Downstream Products

1082113-82-3Relevant articles and documents

Synthesis, local anaesthetic and antiarrhythmic activities of N-alkyl derivatives of proline anilides

Kalinin, Dmitrii V.,Pantsurkin, Vladimir I.,Syropyatov, Boris Ya.,Kalinina, Svetlana A.,Rudakova, Irina P.,Vakhrin, Mikhail I.,Dolzhenko, Anton V.

, p. 144 - 150 (2013/07/27)

We describe here the design, synthesis and evaluation of in vivo local anaesthetic and antiarrhythmic activities of a series of N-alkylproline anilides. Most of the compounds demonstrated surface anaesthetic activity higher than that of lidocaine, ropivacaine and bupivacaine. We established that the local anaesthetic activity was sensitive to structural variations in the substitution pattern at the aromatic ring and the type of alkyl group at the proline nitrogen atom. Some of the prepared N-alkylproline anilides possessed significant antiarrhythmic activity with higher therapeutic indexes than the reference drugs.

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