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CAS

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113473-13-5

Propanal, 2,3-bis(acetyloxy)-, 1-[(2,4-dinitrophenyl)hydrazone], (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113473-13-5 Structure

  • Basic information

    1. Product Name: Propanal, 2,3-bis(acetyloxy)-, 1-[(2,4-dinitrophenyl)hydrazone], (S)-
    2. Synonyms:
    3. CAS NO:113473-13-5
    4. Molecular Formula: C13H14N4O8
    5. Molecular Weight: 354.276
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113473-13-5.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: Propanal, 2,3-bis(acetyloxy)-, 1-[(2,4-dinitrophenyl)hydrazone], (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Propanal, 2,3-bis(acetyloxy)-, 1-[(2,4-dinitrophenyl)hydrazone], (S)-(113473-13-5)
    11. EPA Substance Registry System: Propanal, 2,3-bis(acetyloxy)-, 1-[(2,4-dinitrophenyl)hydrazone], (S)-(113473-13-5)

  • 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: 113473-13-5(Hazardous Substances Data)

113473-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113473-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,7 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113473-13:
(8*1)+(7*1)+(6*3)+(5*4)+(4*7)+(3*3)+(2*1)+(1*3)=95
95 % 10 = 5
So 113473-13-5 is a valid CAS Registry Number.

113473-13-5Downstream Products

113473-13-5Relevant articles and documents

Asymmetric dihydroxylation of acrolein acetals: Synthesis of stable equivalents of Enantiopure glyceraldehyde and glycidaldehyde

Oi, Ryu,Sharpless, K. Barry

, p. 2095 - 2098 (1992)

Asymmetric dihydroxylation (ADH) of acrolein acetals afforded optically active glyceraldehyde equivalents. Enantiopure 3-(1,2-dihydroxyethyl)-1,5-dihydro-3H-2,4-benzodioxepine 3, a protected glyceraldehyde, was obtained from the corresponding acrolein acetal 2 by ADH and subsequent recrystallization. Enantiopure 3-(1,2-epoxyethyl)-1,5-dihydro-3H-2,4-benzodioxepine 5, a protected glycidaldehyde, was produced in two steps from 3.

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