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benzo[d]oxazol-2-yl(o-tolyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1258498-71-3 Structure
  • Basic information

    1. Product Name: benzo[d]oxazol-2-yl(o-tolyl)methanone
    2. Synonyms: benzo[d]oxazol-2-yl(o-tolyl)methanone
    3. CAS NO:1258498-71-3
    4. Molecular Formula:
    5. Molecular Weight: 237.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1258498-71-3.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: benzo[d]oxazol-2-yl(o-tolyl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzo[d]oxazol-2-yl(o-tolyl)methanone(1258498-71-3)
    11. EPA Substance Registry System: benzo[d]oxazol-2-yl(o-tolyl)methanone(1258498-71-3)
  • 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: 1258498-71-3(Hazardous Substances Data)

1258498-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258498-71-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,4,9 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1258498-71:
(9*1)+(8*2)+(7*5)+(6*8)+(5*4)+(4*9)+(3*8)+(2*7)+(1*1)=203
203 % 10 = 3
So 1258498-71-3 is a valid CAS Registry Number.

1258498-71-3Downstream Products

1258498-71-3Relevant articles and documents

Organocatalytic C-H bond arylation of aldehydes to bis-heteroaryl ketones

Toh, Qiao Yan,McNally, Andrew,Vera, Silvia,Erdmann, Nico,Gaunt, Matthew J.

supporting information, p. 3772 - 3775 (2013/04/24)

An organocatalytic aldehyde C-H bond arylation process for the synthesis of complex heteroaryl ketones has been developed. By exploiting the inherent electrophilicity of diaryliodonium salts, we have found that a commercial N-heterocyclic carbene catalyst promotes the union of heteroaryl aldehydes and these heteroaromatic electrophile equivalents in good yields. This straightforward catalytic protocol offers access to ketones bearing a diverse array of arene and heteroarene substituents that can subsequently be converted into molecules displaying structural motifs commonly found in medicinal agents.

Palladium-catalyzed carbonylative C-H activation of heteroarenes

Wu, Xiao-Feng,Anbarasan, Pazhamalai,Neumann, Helfried,Beller, Matthias

supporting information; experimental part, p. 7316 - 7319 (2010/11/05)

Not only carbonylation: The first carbonylative cross-coupling reactions towards ketones using C-H activation have been developed. Various heteroarenes, such as oxazoles, thiazoles, and imidazoles were used as coupling partners in this methodology. DBU =

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