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CAS

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846542-06-1

Butanal, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-(phenylmethoxy)-, (2S,3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 846542-06-1 Structure

  • Basic information

    1. Product Name: Butanal, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-(phenylmethoxy)-, (2S,3R)-
    2. Synonyms:
    3. CAS NO:846542-06-1
    4. Molecular Formula: C17H28O3Si
    5. Molecular Weight: 308.493
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 846542-06-1.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: Butanal, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-(phenylmethoxy)-, (2S,3R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanal, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-(phenylmethoxy)-, (2S,3R)-(846542-06-1)
    11. EPA Substance Registry System: Butanal, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-(phenylmethoxy)-, (2S,3R)-(846542-06-1)

  • 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: 846542-06-1(Hazardous Substances Data)

846542-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 846542-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,6,5,4 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 846542-06:
(8*8)+(7*4)+(6*6)+(5*5)+(4*4)+(3*2)+(2*0)+(1*6)=181
181 % 10 = 1
So 846542-06-1 is a valid CAS Registry Number.

846542-06-1Relevant articles and documents

A SuperQuat glycolate aldol approach to the asymmetric synthesis of hexose monosaccharides

Davies, Stephen G.,Nicholson, Rebecca L.,Smith, Andrew D.

, p. 348 - 359 (2007/10/03)

A stereoselective two-carbon homologation protocol has been developed and applied to the asymmetric synthesis of the hexose monosaccharides D-galactose, D-fucose, D-idose, D-6-deoxyidose, D-talose and D-6-deoxytalose.

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