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CAS

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247042-38-2

(S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 247042-38-2 Structure

  • Basic information

    1. Product Name: (S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one
    2. Synonyms: (S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one
    3. CAS NO:247042-38-2
    4. Molecular Formula:
    5. Molecular Weight: 442.584
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 247042-38-2.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: (S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one(247042-38-2)
    11. EPA Substance Registry System: (S)-3,4-dibenzoyloxy-1-(tert-butyldimethylsilyloxy)butan-2-one(247042-38-2)

  • 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: 247042-38-2(Hazardous Substances Data)

247042-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 247042-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,0,4 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 247042-38:
(8*2)+(7*4)+(6*7)+(5*0)+(4*4)+(3*2)+(2*3)+(1*8)=122
122 % 10 = 2
So 247042-38-2 is a valid CAS Registry Number.

247042-38-2Downstream Products

247042-38-2Relevant articles and documents

Influence of the protecting groups on the syn/anti stereoselectivity of boron aldol additions with erythrulose derivatives. A theoretical and experimental study

Murga, Juan,Falomir, Eva,González, Florenci,Carda, Miguel,Marco

, p. 9697 - 9707 (2007/10/03)

We have investigated a series of aldol additions of protected L-erythrulose derivatives mediated by dicyclohexyl boron chloride. The syn/anti stereoselectivity has been found to depend on the type of protecting groups on the hydroxyl functions at C-3 and

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