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1269005-91-5

4-bromo-N-methyl-N-((trimethylsilyl)methyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1269005-91-5 Structure

  • Basic information

    1. Product Name: 4-bromo-N-methyl-N-((trimethylsilyl)methyl)aniline
    2. Synonyms: 4-bromo-N-methyl-N-((trimethylsilyl)methyl)aniline
    3. CAS NO:1269005-91-5
    4. Molecular Formula:
    5. Molecular Weight: 272.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1269005-91-5.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: 4-bromo-N-methyl-N-((trimethylsilyl)methyl)aniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-bromo-N-methyl-N-((trimethylsilyl)methyl)aniline(1269005-91-5)
    11. EPA Substance Registry System: 4-bromo-N-methyl-N-((trimethylsilyl)methyl)aniline(1269005-91-5)

  • 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: 1269005-91-5(Hazardous Substances Data)

1269005-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1269005-91-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,0,0 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1269005-91:
(9*1)+(8*2)+(7*6)+(6*9)+(5*0)+(4*0)+(3*5)+(2*9)+(1*1)=155
155 % 10 = 5
So 1269005-91-5 is a valid CAS Registry Number.

1269005-91-5Downstream Products

1269005-91-5Relevant articles and documents

Enantioselective conjugate additions of α-amino radicals via cooperative photoredox and Lewis acid catalysis

Ruiz Espelt, Laura,McPherson, Iain S.,Wiensch, Eric M.,Yoon, Tehshik P.

, p. 2452 - 2455 (2015)

We report the highly enantioselective addition of photogenerated α-amino radicals to Michael acceptors. This method features a dual-catalyst protocol that combines transition metal photoredox catalysis with chiral Lewis acid catalysis. The combination of these two powerful modes of catalysis provides an effective, general strategy to generate and control the reactivity of photogenerated reactive intermediates.

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