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ethyl 3-(4-chlorophenyl)-4-oxopentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 66203-72-3 Structure
  • Basic information

    1. Product Name: ethyl 3-(4-chlorophenyl)-4-oxopentanoate
    2. Synonyms: ethyl 3-(4-chlorophenyl)-4-oxopentanoate
    3. CAS NO:66203-72-3
    4. Molecular Formula:
    5. Molecular Weight: 254.713
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 66203-72-3.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: ethyl 3-(4-chlorophenyl)-4-oxopentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 3-(4-chlorophenyl)-4-oxopentanoate(66203-72-3)
    11. EPA Substance Registry System: ethyl 3-(4-chlorophenyl)-4-oxopentanoate(66203-72-3)
  • 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: 66203-72-3(Hazardous Substances Data)

66203-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66203-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,0 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66203-72:
(7*6)+(6*6)+(5*2)+(4*0)+(3*3)+(2*7)+(1*2)=113
113 % 10 = 3
So 66203-72-3 is a valid CAS Registry Number.

66203-72-3Upstream product

66203-72-3Downstream Products

66203-72-3Relevant articles and documents

Engineering Dirhodium Artificial Metalloenzymes for Diazo Coupling Cascade Reactions**

Bultman, Max J.,Huang, Rui,Lewis, Jared C.,Li, Ying,Roux, Benoit,Upp, David M.

, p. 23672 - 23677 (2021)

Artificial metalloenzymes (ArMs) are commonly used to control the stereoselectivity of catalytic reactions, but controlling chemoselectivity remains challenging. In this study, we engineer a dirhodium ArM to catalyze diazo cross-coupling to form an alkene that, in a one-pot cascade reaction, is reduced to an alkane with high enantioselectivity (typically >99 % ee) by an alkene reductase. The numerous protein and small molecule components required for the cascade reaction had minimal effect on ArM catalysis. Directed evolution of the ArM led to improved yields and E/Z selectivities for a variety of substrates, which translated to cascade reaction yields. MD simulations of ArM variants were used to understand the structural role of the cofactor on ArM conformational dynamics. These results highlight the ability of ArMs to control both catalyst stereoselectivity and chemoselectivity to enable reactions in complex media that would otherwise lead to undesired side reactions.

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