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<3-(2-methoxyphenyl)-1-propynyl>trimethylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107941-23-1 Structure
  • Basic information

    1. Product Name: <3-(2-methoxyphenyl)-1-propynyl>trimethylsilane
    2. Synonyms: <3-(2-methoxyphenyl)-1-propynyl>trimethylsilane
    3. CAS NO:107941-23-1
    4. Molecular Formula:
    5. Molecular Weight: 218.371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107941-23-1.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: <3-(2-methoxyphenyl)-1-propynyl>trimethylsilane(CAS DataBase Reference)
    10. NIST Chemistry Reference: <3-(2-methoxyphenyl)-1-propynyl>trimethylsilane(107941-23-1)
    11. EPA Substance Registry System: <3-(2-methoxyphenyl)-1-propynyl>trimethylsilane(107941-23-1)
  • 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: 107941-23-1(Hazardous Substances Data)

107941-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107941-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,4 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107941-23:
(8*1)+(7*0)+(6*7)+(5*9)+(4*4)+(3*1)+(2*2)+(1*3)=121
121 % 10 = 1
So 107941-23-1 is a valid CAS Registry Number.

107941-23-1Relevant articles and documents

Cobalt-catalyzed benzyl-alkynyl coupling

Kuno, Akiko,Saino, Naoko,Kamachi, Taku,Okamoto, Sentaro

, p. 2591 - 2594 (2006)

Benzylic halides coupled with 1-alkynylmagnesium halides in the presence of a catalytic amount of Co(acac)3 to provide 1-aryl-2-alkynes in moderate to good yield.

Ortho-Bromo(propa-1,2-dien-1-yl)arenes: Substrates for domino reactions

Masters, Kye-Simeon,Wallesch, Manuela,Braese, Stefan

experimental part, p. 9060 - 9067 (2011/12/03)

o-Bromo(propa-1,2-dien-1-yl)arenes exhibit novel and orthogonal reactivity under Pd catalysis in the presence of secondary amines to form enamines (concerted Pd insertion, intramolecular carbopalladation, and terminative Buchwald-Hartwig coupling) and of amides to form indoles (addition, Buchwald-Hartwig cyclization, and loss of the acetyl group). The substrates for these reactions can be accessed in a reliable and highly selective two-step process from 2-bromoaryl bromides.

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