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CAS

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1447965-43-6

2-(2-(naphthalene-1-yl)-3-tosyloxazolidin-4-yl)-1-(thiophen-2-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1447965-43-6 Structure

  • Basic information

    1. Product Name: 2-(2-(naphthalene-1-yl)-3-tosyloxazolidin-4-yl)-1-(thiophen-2-yl)ethanone
    2. Synonyms:
    3. CAS NO:1447965-43-6
    4. Molecular Formula:
    5. Molecular Weight: 477.605
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1447965-43-6.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: 2-(2-(naphthalene-1-yl)-3-tosyloxazolidin-4-yl)-1-(thiophen-2-yl)ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-(naphthalene-1-yl)-3-tosyloxazolidin-4-yl)-1-(thiophen-2-yl)ethanone(1447965-43-6)
    11. EPA Substance Registry System: 2-(2-(naphthalene-1-yl)-3-tosyloxazolidin-4-yl)-1-(thiophen-2-yl)ethanone(1447965-43-6)

  • 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: 1447965-43-6(Hazardous Substances Data)

1447965-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1447965-43-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,7,9,6 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1447965-43:
(9*1)+(8*4)+(7*4)+(6*7)+(5*9)+(4*6)+(3*5)+(2*4)+(1*3)=206
206 % 10 = 6
So 1447965-43-6 is a valid CAS Registry Number.

1447965-43-6Downstream Products

1447965-43-6Relevant articles and documents

Asymmetric synthesis of 1,3-oxazolidines via intramolecular aza-michael addition by bifunctional organocatalysts

Fukata, Yukihiro,Asano, Keisuke,Matsubara, Seijiro

supporting information, p. 355 - 357 (2013/05/09)

A novel synthetic route to optically active 1,3-oxazolidines via formal [3 + 2] cycloaddition in the presence of cinchonaalkaloid- thiourea-based bifunctional organocatalysts is reported. This protocol gives easy access to a wide range of chiral 1,3- oxazolidines. In addition, the results show that bifunctional organocatalysts can effect the intramolecular aza-Michael addition, leading to the asymmetric synthesis of nitrogencontaining heterocycles.

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