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CAS

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616867-25-5

Butanoic acid, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,3-dimethyl-, (2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 616867-25-5 Structure

  • Basic information

    1. Product Name: Butanoic acid, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,3-dimethyl-, (2R)-
    2. Synonyms:
    3. CAS NO:616867-25-5
    4. Molecular Formula: C23H32O3Si
    5. Molecular Weight: 384.591
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 616867-25-5.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: Butanoic acid, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,3-dimethyl-, (2R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanoic acid, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,3-dimethyl-, (2R)-(616867-25-5)
    11. EPA Substance Registry System: Butanoic acid, 2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,3-dimethyl-, (2R)-(616867-25-5)

  • 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: 616867-25-5(Hazardous Substances Data)

616867-25-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 616867-25-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,6,8,6 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 616867-25:
(8*6)+(7*1)+(6*6)+(5*8)+(4*6)+(3*7)+(2*2)+(1*5)=185
185 % 10 = 5
So 616867-25-5 is a valid CAS Registry Number.

616867-25-5Relevant articles and documents

A stereodivergent approach to chiral nonracemic N-protected α,α-dialkylated amino acids

Spino, Claude,Gobdout, Cedrickx

, p. 12106 - 12107 (2007/10/03)

Menthyl carboxaldehyde is used as a chiral auxiliary to make quaternary amino acids of either configuration via a stereodivergent approach that includes an SN2′ displacement by a cuprate reagent and a Curtius rearrangement as key steps. Copyright

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