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20577-36-0

3-Buten-1-one, 2-ethyl-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 20577-36-0 Structure

  • Basic information

    1. Product Name: 3-Buten-1-one, 2-ethyl-1-phenyl-
    2. Synonyms:
    3. CAS NO:20577-36-0
    4. Molecular Formula: C12H14O
    5. Molecular Weight: 174.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20577-36-0.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: 3-Buten-1-one, 2-ethyl-1-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Buten-1-one, 2-ethyl-1-phenyl-(20577-36-0)
    11. EPA Substance Registry System: 3-Buten-1-one, 2-ethyl-1-phenyl-(20577-36-0)

  • 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: 20577-36-0(Hazardous Substances Data)

20577-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20577-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,7 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20577-36:
(7*2)+(6*0)+(5*5)+(4*7)+(3*7)+(2*3)+(1*6)=100
100 % 10 = 0
So 20577-36-0 is a valid CAS Registry Number.

20577-36-0Downstream Products

20577-36-0Relevant articles and documents

Alkyne hydroacylation: Switching regioselectivity by tandem ruthenium catalysis

Chen, Qing-An,Cruz, Faben A.,Dong, Vy M.

supporting information, p. 3157 - 3160 (2015/03/30)

By using tandem Ru-catalysis, internal alkynes can be coupled with aldehydes for the synthesis of β,γ-unsaturated ketones. The catalyst promotes alkyne transformations with high regioselectivity, with examples that include the differentiation of a methyl vs ethyl substituent on the alkyne. Mechanistic studies suggest that the regioselectivity results from a selective allene formation that is governed by allylic strain.

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