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CAS

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273216-89-0

6,6′-bis[4-phenyloxazolin-2-y1]-2,2′-bipyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 6,6'-bis[(4S)-4-phenyl-4,5-dihydro-1,3-oxazol-2-yl]-2,2'-bipyridine

    Cas No: 273216-89-0

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  • 273216-89-0 Structure

  • Basic information

    1. Product Name: 6,6′-bis[4-phenyloxazolin-2-y1]-2,2′-bipyridine
    2. Synonyms:
    3. CAS NO:273216-89-0
    4. Molecular Formula:
    5. Molecular Weight: 446.508
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 273216-89-0.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: 6,6′-bis[4-phenyloxazolin-2-y1]-2,2′-bipyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,6′-bis[4-phenyloxazolin-2-y1]-2,2′-bipyridine(273216-89-0)
    11. EPA Substance Registry System: 6,6′-bis[4-phenyloxazolin-2-y1]-2,2′-bipyridine(273216-89-0)

  • 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: 273216-89-0(Hazardous Substances Data)

273216-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 273216-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,3,2,1 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 273216-89:
(8*2)+(7*7)+(6*3)+(5*2)+(4*1)+(3*6)+(2*8)+(1*9)=140
140 % 10 = 0
So 273216-89-0 is a valid CAS Registry Number.

273216-89-0Downstream Products

273216-89-0Relevant articles and documents

Enantioselective Aromatic Sulfide Oxidation and Tandem Kinetic Resolution Using Aqueous H2O2 and Chiral Iron–Bis(oxazolinyl)bipyridine Catalysts

Jalba, Angela,Régnier, Noémie,Ollevier, Thierry

, p. 1628 - 1637 (2017/04/06)

An efficient method for the oxidation of aromatic sulfides has been developed by using aqueous H2O2, catalyzed by the in situ generated chiral Fe/6,6′-bis(4-isopropyloxazolin-2-yl)-2,2′-bipyridine (bipybox-iPr) complex. The corresponding sulfoxides were obtained with high enantioselectivities (up to 98.5:1.5 er) and in good yields (up to 61 %) when the mono-oxidation of the sulfides was performed in combination with the kinetic resolution of the sulfoxide into the sulfone.

Asymmetric hetero-Diels-Alder reaction of glyoxylate esters and Danishefsky's diene catalyzed by chiral bis(oxazoline)-lanthanide complexes

Qian, Changtao,Wang, Longcheng

, p. 2203 - 2206 (2007/10/03)

Asymmetric hetero-Diels-Alder reactions of glyoxylate esters and Danishefsky's diene catalyzed by various chiral bis(oxazoline)-lanthanide complexes afforded the corresponding aldol adducts, which upon treatment with trifluoroacetic acid, furnished the he

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