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120963-42-0

(-)-3-ethoxy-N-cyclopentyl>carbamoyl>propenamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 120963-42-0 Structure

  • Basic information

    1. Product Name: (-)-3-ethoxy-N-cyclopentyl>carbamoyl>propenamide
    2. Synonyms: (-)-3-ethoxy-N-cyclopentyl>carbamoyl>propenamide
    3. CAS NO:120963-42-0
    4. Molecular Formula:
    5. Molecular Weight: 418.447
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120963-42-0.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: (-)-3-ethoxy-N-cyclopentyl>carbamoyl>propenamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-3-ethoxy-N-cyclopentyl>carbamoyl>propenamide(120963-42-0)
    11. EPA Substance Registry System: (-)-3-ethoxy-N-cyclopentyl>carbamoyl>propenamide(120963-42-0)

  • 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: 120963-42-0(Hazardous Substances Data)

120963-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120963-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,6 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120963-42:
(8*1)+(7*2)+(6*0)+(5*9)+(4*6)+(3*3)+(2*4)+(1*2)=110
110 % 10 = 0
So 120963-42-0 is a valid CAS Registry Number.

120963-42-0Relevant articles and documents

Synthesis and Antiviral Activity of the Enantiomeric Forms of Carba-5-iodo-2'-deoxyuridine and Carba-(E)-5-(2-bromovinyl)-2'-deoxyuridine

Balzarini, Jan,Baumgartner, Harald,Bodenteich, Michael,Clercq, Erik De,Griengl, Herfried

, p. 1861 - 1865 (2007/10/02)

Both enantiomers of the carbocyclic analogues of 5-iodo-2'-deoxyuridine (14 and ent-14) and of (E)-5-(2-bromovinyl)-2'-deoxyuridine (16 and ent-16) were synthesized by using (+)- or (-)-endo-norborn-5-en-2-yl acetate or butyrate, respectively, as starting

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