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Benzaldehyde, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-4,6-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 388570-83-0 Structure
  • Basic information

    1. Product Name: Benzaldehyde, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-4,6-dimethoxy-
    2. Synonyms:
    3. CAS NO:388570-83-0
    4. Molecular Formula: C26H30O4Si
    5. Molecular Weight: 434.607
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 388570-83-0.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: Benzaldehyde, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-4,6-dimethoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzaldehyde, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-4,6-dimethoxy-(388570-83-0)
    11. EPA Substance Registry System: Benzaldehyde, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-4,6-dimethoxy-(388570-83-0)
  • 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: 388570-83-0(Hazardous Substances Data)

388570-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 388570-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,8,5,7 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 388570-83:
(8*3)+(7*8)+(6*8)+(5*5)+(4*7)+(3*0)+(2*8)+(1*3)=200
200 % 10 = 0
So 388570-83-0 is a valid CAS Registry Number.

388570-83-0Relevant articles and documents

4-(Trialkylsilyl)oxybut-2-ynals as dienophiles in the Diels-Alder synthesis of α-(hydroxymethyl)benzaldehydes

Morrison, Christopher F,Burnell

, p. 7367 - 7369 (2007/10/03)

The α-(hydroxymethyl)benzaldehyde derivative 2 has been synthesized by heating ynal 3 with diene 5, which produced the α-(silyloxymethyl)benzaldehyde 6 by a Diels-Alder/retro-Diels-Alder process, followed by methylation, thioacetalization, and removal of the silyl protecting group. Decarbonylation of α-(silyloxymethyl)benzaldehydes 6 and 10 takes place readily in the presence of zinc(II) chloride or para-toluenesulfonic acid.

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