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96569-80-1

Benzene, [1-(methoxymethoxy)ethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 96569-80-1 Structure

  • Basic information

    1. Product Name: Benzene, [1-(methoxymethoxy)ethenyl]-
    2. Synonyms:
    3. CAS NO:96569-80-1
    4. Molecular Formula: C10H12O2
    5. Molecular Weight: 164.204
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 96569-80-1.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: Benzene, [1-(methoxymethoxy)ethenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [1-(methoxymethoxy)ethenyl]-(96569-80-1)
    11. EPA Substance Registry System: Benzene, [1-(methoxymethoxy)ethenyl]-(96569-80-1)

  • 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: 96569-80-1(Hazardous Substances Data)

96569-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96569-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,6 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96569-80:
(7*9)+(6*6)+(5*5)+(4*6)+(3*9)+(2*8)+(1*0)=191
191 % 10 = 1
So 96569-80-1 is a valid CAS Registry Number.

96569-80-1Relevant articles and documents

Acid catalyzed rearrangement of vinyl and ketene acetals

Maziarz, Elzbieta,Furman, Bart?omiej

, p. 1651 - 1658 (2014/02/14)

Substituted vinyl and ketene acetals undergo smooth oxygen-to-carbon rearrangement with a catalytic amount of TMSOTf to afford chain-extended ketones or esters, respectively. The developed procedure has been applied to the stereoselective synthesis of C-glycosides from the corresponding anomeric vinyl ethers.

HETEROATOM DIRECTED Β-LITHIATION OF A VINYL ETHER

McDougal, Patrick G.,Rico, Joseph G.

, p. 5977 - 5980 (2007/10/02)

Oxygen directed β-deprotonation of a vinyl ether leads to Z substituted enol ethers.The stereoselective elaboration to a naturally occuring threo 1,3-diol is described.

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