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CAS

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1228844-66-3

C20H21BrO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1228844-66-3 Structure

  • Basic information

    1. Product Name: C20H21BrO3
    2. Synonyms: C20H21BrO3
    3. CAS NO:1228844-66-3
    4. Molecular Formula:
    5. Molecular Weight: 389.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1228844-66-3.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: C20H21BrO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H21BrO3(1228844-66-3)
    11. EPA Substance Registry System: C20H21BrO3(1228844-66-3)

  • 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: 1228844-66-3(Hazardous Substances Data)

1228844-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1228844-66-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,8,4 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1228844-66:
(9*1)+(8*2)+(7*2)+(6*8)+(5*8)+(4*4)+(3*4)+(2*6)+(1*6)=173
173 % 10 = 3
So 1228844-66-3 is a valid CAS Registry Number.

1228844-66-3Downstream Products

1228844-66-3Relevant articles and documents

Synthesis of enantiomerically enriched α,α-disubstituted β,γ-epoxy esters using hydrolytic kinetic resolution catalyzed by salenCo(III)

Viera, Ignacio,Manta, Eduardo,Gonzalez, Lucia,Mahler, Graciela

, p. 631 - 635 (2010)

Novel α,α-disubstituted epoxy esters were prepared in enantiopure form by hydrolytic kinetic resolution (HKR) of the corresponding racemic mixtures using chiral salenCo(III) as catalyst. The methodology provides a convenient route to enantioenriched β,γ-epoxy esters 2a, 2c and 2d.

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