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1033620-20-0

C64H89NO5P2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1033620-20-0 Structure

  • Basic information

    1. Product Name: C64H89NO5P2
    2. Synonyms: C64H89NO5P2
    3. CAS NO:1033620-20-0
    4. Molecular Formula:
    5. Molecular Weight: 1014.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1033620-20-0.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: C64H89NO5P2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C64H89NO5P2(1033620-20-0)
    11. EPA Substance Registry System: C64H89NO5P2(1033620-20-0)

  • 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: 1033620-20-0(Hazardous Substances Data)

1033620-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1033620-20-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,6,2 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1033620-20:
(9*1)+(8*0)+(7*3)+(6*3)+(5*6)+(4*2)+(3*0)+(2*2)+(1*0)=90
90 % 10 = 0
So 1033620-20-0 is a valid CAS Registry Number.

1033620-20-0Downstream Products

1033620-20-0Relevant articles and documents

Screening of a phosphite-phosphoramidite ligand library for palladium-catalysed asymmetric allylic substitution reactions: The origin of enantioselectivity

Pamies, Oscar,Dieguez, Montserrat

, p. 944 - 960 (2008)

We have designed a new library of readily available, highly modular phosphite-phosphoramidite ligands for asymmetric allylic substitution reactions. They are easily prepared in one step from commercially available chiral 1,2-amino alcohols. The introduction of a phosphoramidite moiety into the ligand design is highly advantageous for the product outcome. This ligand library affords high reaction rates (TOFs of up to 800 mol (mol h)-1) and enantioselectivities (ees of up to 99%) and, at the same time, contains a broad range of disubstituted hindered and unhindered substrate types. NMR study of the Pd-π-allyl intermediates provide a deeper understanding of the effect of the ligand parameters on the origin of cnantioselectivity.

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