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65611-10-1

Ethane, 1,2-dichloro-1,2-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65611-10-1 Structure

  • Basic information

    1. Product Name: Ethane, 1,2-dichloro-1,2-dimethoxy-
    2. Synonyms:
    3. CAS NO:65611-10-1
    4. Molecular Formula: C4H8Cl2O2
    5. Molecular Weight: 159.012
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65611-10-1.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: Ethane, 1,2-dichloro-1,2-dimethoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethane, 1,2-dichloro-1,2-dimethoxy-(65611-10-1)
    11. EPA Substance Registry System: Ethane, 1,2-dichloro-1,2-dimethoxy-(65611-10-1)

  • 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: 65611-10-1(Hazardous Substances Data)

65611-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65611-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,1 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65611-10:
(7*6)+(6*5)+(5*6)+(4*1)+(3*1)+(2*1)+(1*0)=111
111 % 10 = 1
So 65611-10-1 is a valid CAS Registry Number.

65611-10-1Relevant articles and documents

DIISOPROPOXY- AND DI-tert-BUTOXYETHYNE STABLE ACETYLENE DIETHERS

Bou, Anna,Pericas,Miquel A.,Serratosa, Felix

, p. 1441 - 1449 (2007/10/02)

The rather stable acetylene diethers diisopropoxy- and di-t-butoxyethyne are prepared either from glyoxal or dioxane.Catalytic hydrogenation, acid-catalyzed hydration and formation of the corresponding hexacarbonyl dicobalt complexes are reported.

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