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CAS

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1228045-65-5

3-(1-hydroxy-3-phenyl-1H-inden-2-yl)oxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1228045-65-5 Structure

  • Basic information

    1. Product Name: 3-(1-hydroxy-3-phenyl-1H-inden-2-yl)oxazolidin-2-one
    2. Synonyms:
    3. CAS NO:1228045-65-5
    4. Molecular Formula:
    5. Molecular Weight: 293.322
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1228045-65-5.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: 3-(1-hydroxy-3-phenyl-1H-inden-2-yl)oxazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(1-hydroxy-3-phenyl-1H-inden-2-yl)oxazolidin-2-one(1228045-65-5)
    11. EPA Substance Registry System: 3-(1-hydroxy-3-phenyl-1H-inden-2-yl)oxazolidin-2-one(1228045-65-5)

  • 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: 1228045-65-5(Hazardous Substances Data)

1228045-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1228045-65-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,0,4 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1228045-65:
(9*1)+(8*2)+(7*2)+(6*8)+(5*0)+(4*4)+(3*5)+(2*6)+(1*5)=135
135 % 10 = 5
So 1228045-65-5 is a valid CAS Registry Number.

1228045-65-5Downstream Products

1228045-65-5Relevant articles and documents

Rhodium-catalyzed annulation of ynamides with bifunctional arylboron reagents

Gourdet, Benoit,Rudkin, Mairi E.,Lam, Hon Wai

, p. 2554 - 2557 (2010)

Annulation of ynamides with arylboronic acids or esters containing an electrophilic functional group at the ortho-position proceeds under the action of rhodium catalysis to generate 2-amidoindenols or 2-amidoindenes, usually with good regioselectivity.

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