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1221065-06-0

dimethyl 2-(2-(benzyloxy)-6-methylbenzylidene)malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1221065-06-0 Structure

  • Basic information

    1. Product Name: dimethyl 2-(2-(benzyloxy)-6-methylbenzylidene)malonate
    2. Synonyms: dimethyl 2-(2-(benzyloxy)-6-methylbenzylidene)malonate
    3. CAS NO:1221065-06-0
    4. Molecular Formula:
    5. Molecular Weight: 340.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1221065-06-0.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: dimethyl 2-(2-(benzyloxy)-6-methylbenzylidene)malonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl 2-(2-(benzyloxy)-6-methylbenzylidene)malonate(1221065-06-0)
    11. EPA Substance Registry System: dimethyl 2-(2-(benzyloxy)-6-methylbenzylidene)malonate(1221065-06-0)

  • 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: 1221065-06-0(Hazardous Substances Data)

1221065-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1221065-06-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,0,6 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1221065-06:
(9*1)+(8*2)+(7*2)+(6*1)+(5*0)+(4*6)+(3*5)+(2*0)+(1*6)=90
90 % 10 = 0
So 1221065-06-0 is a valid CAS Registry Number.

1221065-06-0Relevant articles and documents

Expeditious synthesis of benzopyrans via lewis acid-catalyzed C-H functionalization: Remarkable enhancement of reactivity by an ortho substituent

Mori, Keiji,Kawasaki, Taro,Sueoka, Shosaku,Akiyama, Takahiko

supporting information; experimental part, p. 1732 - 1735 (2010/09/05)

An expeditious construction of a benzopyran skeleton via Lewis acid-catalyzed C-H functionalization was achieved. In this process, a [1,5] hydride shift and 6-endo cyclization successively occurred to give benzopyrans. The presence of substituents ortho to the alkoxy group significantly enhanced the reactivity, affording the desired compounds in excellent chemical yields with short reaction times.

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