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92573-80-3

Benzeneacetaldehyde, a-[(tetrahydro-2H-pyran-2-yl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92573-80-3 Structure

  • Basic information

    1. Product Name: Benzeneacetaldehyde, a-[(tetrahydro-2H-pyran-2-yl)oxy]-
    2. Synonyms:
    3. CAS NO:92573-80-3
    4. Molecular Formula: C13H16O3
    5. Molecular Weight: 220.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92573-80-3.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: Benzeneacetaldehyde, a-[(tetrahydro-2H-pyran-2-yl)oxy]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneacetaldehyde, a-[(tetrahydro-2H-pyran-2-yl)oxy]-(92573-80-3)
    11. EPA Substance Registry System: Benzeneacetaldehyde, a-[(tetrahydro-2H-pyran-2-yl)oxy]-(92573-80-3)

  • 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: 92573-80-3(Hazardous Substances Data)

92573-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92573-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,7 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92573-80:
(7*9)+(6*2)+(5*5)+(4*7)+(3*3)+(2*8)+(1*0)=153
153 % 10 = 3
So 92573-80-3 is a valid CAS Registry Number.

92573-80-3Relevant articles and documents

Au-catalyzed intramolecular hydroalkoxylation of gem-difluorinated alkynols

Hamel, Jean-Denys,Paquin, Jean-Fran?ois

, p. 11 - 23 (2018/10/20)

The intramolecular hydroalkoxylation of gem-difluorinated alkynols was found possible under Au catalysis, allowing for the preparation of a series of fluorinated heterocycles. The nature of the solvent was found to be especially critical in the cyclizatio

NOVEL SYNTHESIS AND APPLICATION OF MIXED ACETALS (ACETYL METHYL ACETALS)

Mandai, Tadakatsu,Irei, Hiroshi,Kawada, Mikio,Otera, Junzo

, p. 2371 - 2374 (2007/10/02)

A novel synthetic method for mixed acetals (acetyl methyl acetals) by electrolysis of hemithioacetals derived from methoxy(phenylthio)methane is newly developed.Synthetic application of these mixed acetals as an aldehyde equivalent is also demonstrated.

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