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CAS

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107600-17-9

N-methyl-N-<(trimethylsilyl)methyl>-2-acetylbenzylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107600-17-9 Structure

  • Basic information

    1. Product Name: N-methyl-N-<(trimethylsilyl)methyl>-2-acetylbenzylamine
    2. Synonyms:
    3. CAS NO:107600-17-9
    4. Molecular Formula:
    5. Molecular Weight: 249.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107600-17-9.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-methyl-N-<(trimethylsilyl)methyl>-2-acetylbenzylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-methyl-N-<(trimethylsilyl)methyl>-2-acetylbenzylamine(107600-17-9)
    11. EPA Substance Registry System: N-methyl-N-<(trimethylsilyl)methyl>-2-acetylbenzylamine(107600-17-9)

  • 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: 107600-17-9(Hazardous Substances Data)

107600-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107600-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,0 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107600-17:
(8*1)+(7*0)+(6*7)+(5*6)+(4*0)+(3*0)+(2*1)+(1*7)=89
89 % 10 = 9
So 107600-17-9 is a valid CAS Registry Number.

107600-17-9Downstream Products

107600-17-9Relevant articles and documents

Rearrangement of (Substituted benzyl)trimethylammonium Ylides in a Nonbasic Medium: The Improved Sommelet-Hauser Rearrangement

Nakano, Mitsuji,Sato, Yoshiro

, p. 1844 - 1847 (2007/10/02)

Benzyl quaternary ammonium ylide formation in a nonbasic medium was accomplished by fluoride anion induced desilylation of benzyldimethylammonium bromide (3a) and ortho- or para-substituted benzyl analogues 3b-k.Treatment of 3 with CsF in HMPA at room temperature gives high yields of the Sommelet-Hauser rearrangement products 7 from 3a and methyl-, acetoxy-, and chloro-substituted analogues 3b-f.However, formation of the Stevens rearrangement products 8 is competitive for the reaction of compounds 3g-k having strong electron-withdrawing substituents such as acetyl, cyano, and nitrogen groups.From the o-cyano-substituted analogue 3h, a considerable amount of para Sommelet-Hauser rearrangement product is isolated.

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