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1644306-10-4

C14(13)C2H18O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1644306-10-4 Structure

  • Basic information

    1. Product Name: C14(13)C2H18O4
    2. Synonyms: C14(13)C2H18O4
    3. CAS NO:1644306-10-4
    4. Molecular Formula:
    5. Molecular Weight: 276.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1644306-10-4.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: C14(13)C2H18O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14(13)C2H18O4(1644306-10-4)
    11. EPA Substance Registry System: C14(13)C2H18O4(1644306-10-4)

  • 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: 1644306-10-4(Hazardous Substances Data)

1644306-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1644306-10-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,4,3,0 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1644306-10:
(9*1)+(8*6)+(7*4)+(6*4)+(5*3)+(4*0)+(3*6)+(2*1)+(1*0)=144
144 % 10 = 4
So 1644306-10-4 is a valid CAS Registry Number.

1644306-10-4Relevant articles and documents

Gold-catalyzed diastereoselective cycloisomerization of alkylidene-cyclopropane-bearing 1,6-diynes

Zheng, Hongchao,Adduci, Laura L.,Felix, Ryan J.,Gagne, Michel R.

supporting information, p. 7904 - 7907 (2014/08/05)

An unprecedented gold-catalyzed diastereoselective cycloisomerization of 1,6-diynes bearing an alkylidene cyclopropane moiety has been developed. This methodology enables rapid access to a variety of 1,2-trimethylenenorbornanes, which are important building blocks in the preparations of abiotic and sesquiterpene core structures. When gold met alkylidenecyclopropane: Cationic gold catalysts can mediate the highly exothermic (≈60 kcal mol-1) cycloisomerization of 1,6-diynes bearing an alkylidene cyclopropane moiety. This diastereoselective methodology efficiently generates 1,2- trimethylenenorbornanes, an important building block for abiotic targets and sesquiterpene natural products. DCE=1,2-dichloroethane, Tf= trifluoromethanesulfonyl, Tol=Tolyl.

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