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1440546-92-8

N-(4-methoxy-2-((trimethylsilyl)ethynyl)phenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1440546-92-8 Structure

  • Basic information

    1. Product Name: N-(4-methoxy-2-((trimethylsilyl)ethynyl)phenyl)acetamide
    2. Synonyms: N-(4-methoxy-2-((trimethylsilyl)ethynyl)phenyl)acetamide
    3. CAS NO:1440546-92-8
    4. Molecular Formula:
    5. Molecular Weight: 261.396
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1440546-92-8.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: N-(4-methoxy-2-((trimethylsilyl)ethynyl)phenyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-methoxy-2-((trimethylsilyl)ethynyl)phenyl)acetamide(1440546-92-8)
    11. EPA Substance Registry System: N-(4-methoxy-2-((trimethylsilyl)ethynyl)phenyl)acetamide(1440546-92-8)

  • 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: 1440546-92-8(Hazardous Substances Data)

1440546-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440546-92-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,0,5,4 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1440546-92:
(9*1)+(8*4)+(7*4)+(6*0)+(5*5)+(4*4)+(3*6)+(2*9)+(1*2)=148
148 % 10 = 8
So 1440546-92-8 is a valid CAS Registry Number.

1440546-92-8Downstream Products

1440546-92-8Relevant articles and documents

Synthesis of 2,3-Disubstituted Indoles and Benzofurans by the Tandem Reaction of Rhodium(II)-Catalyzed Intramolecular C-H Insertion and Oxygen-Mediated Oxidation

Shen, Hongjuan,Fu, Junkai,Yuan, Hao,Gong, Jianxian,Yang, Zhen

, p. 10180 - 10192 (2016/11/17)

A highly effective and straightforward method to construct a wide range of functionalized 2,3-disubstituted indoles has been developed. The method involves the tandem reaction of rhodium(II)-catalyzed denitrogenative annulation of triazole-based benzyl an

Amphipathic α-helix mimetics based on a 1,2-diphenylacetylene scaffold

Jung, Kwan-Young,Vanommeslaeghe, Kenno,Lanning, Maryanna E.,Yap, Jeremy L.,Gordon, Caryn,Wilder, Paul T.,Mackerell, Alexander D.,Fletcher, Steven

, p. 3234 - 3237 (2013/07/26)

In order to mimic amphipathic α-helices, a novel scaffold based on a 1,2-diphenylacetylene was designed. NMR and computational modeling confirmed that an intramolecular hydrogen bond favors conformations of the 1,2-diphenylacetylene that allow for accurat

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