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1020738-09-3

C19H18N2O7 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1020738-09-3 Structure

  • Basic information

    1. Product Name: C19H18N2O7
    2. Synonyms:
    3. CAS NO:1020738-09-3
    4. Molecular Formula:
    5. Molecular Weight: 386.361
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1020738-09-3.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: C19H18N2O7(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H18N2O7(1020738-09-3)
    11. EPA Substance Registry System: C19H18N2O7(1020738-09-3)

  • 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: 1020738-09-3(Hazardous Substances Data)

1020738-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1020738-09-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,7,3 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1020738-09:
(9*1)+(8*0)+(7*2)+(6*0)+(5*7)+(4*3)+(3*8)+(2*0)+(1*9)=103
103 % 10 = 3
So 1020738-09-3 is a valid CAS Registry Number.

1020738-09-3Downstream Products

1020738-09-3Relevant articles and documents

Diastereoselective ru-catalyzed cross-metathesis-dihydroxylation sequence. An efficient approach toward enantiomerically enriched syn-diols

Neisius, N. Matthias,Plietker, Bernd

, p. 3218 - 3227 (2008)

(Chemical Equation Presented) Sequential catalysis has evolved as a powerful concept within the past years and allows the more efficient use of catalytically active expensive transition metals in organic synthesis. In this paper we present the stereoselective cross-metathesis-dihydroxylation of various olefins with chiral auxiliary substituted acrylamides. The chiral information (i.e., the auxiliary) introduced in the metathesis reactions allows for a stereoselective subsequent RuO4-catalyzed dihydroxylation. The sequence is concluded by an unusual kinetic resolution of the diastereomeric diols obtained in the oxidation reaction. As a consequence a variety of structurally diverse enantiomerically enriched diols are obtained. To the best of our knowledge the results summarized in this paper represent the first highly efficient diastereoselective RuO4-catalyzed oxidation.

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