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1233735-47-1

2-hydroxy-1-(1-phenyl-1H-imidazol-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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  • 1233735-47-1 Structure

  • Basic information

    1. Product Name: 2-hydroxy-1-(1-phenyl-1H-imidazol-2-yl)ethanone
    2. Synonyms: 2-hydroxy-1-(1-phenyl-1H-imidazol-2-yl)ethanone
    3. CAS NO:1233735-47-1
    4. Molecular Formula:
    5. Molecular Weight: 202.213
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1233735-47-1.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-hydroxy-1-(1-phenyl-1H-imidazol-2-yl)ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-hydroxy-1-(1-phenyl-1H-imidazol-2-yl)ethanone(1233735-47-1)
    11. EPA Substance Registry System: 2-hydroxy-1-(1-phenyl-1H-imidazol-2-yl)ethanone(1233735-47-1)

  • 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: 1233735-47-1(Hazardous Substances Data)

1233735-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1233735-47-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,7,3 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1233735-47:
(9*1)+(8*2)+(7*3)+(6*3)+(5*7)+(4*3)+(3*5)+(2*4)+(1*7)=141
141 % 10 = 1
So 1233735-47-1 is a valid CAS Registry Number.

1233735-47-1Relevant articles and documents

Palladium-catalyzed asymmetric allylic alkylation of 2-acylimidazoles as ester enolate equivalents

Trost, Barry M.,Lehr, Konrad,Michaelis, David J.,Xu, Jiayi,Buckl, Andreas K.

, p. 8915 - 8917 (2010)

A broad range of highly enantioenriched 2-acylimidazoles are synthesized by palladium-catalyzed decarboxylative asymmetric allylic alkylation (DAAA) of 2-imidazolo-substituted enol carbonates. The enantioenriched 2-acylimidazole products can easily be converted to the corresponding carboxylic acid, ester, amide, and ketone derivatives with complete retention of the enantiopurity. The synthetic utility of this new method is demonstrated in the short, efficient synthesis of cetiedil.

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