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Methanamine, N,N-dimethyl-1-(methyldiphenylsilyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54926-32-8 Structure
  • Basic information

    1. Product Name: Methanamine, N,N-dimethyl-1-(methyldiphenylsilyl)-
    2. Synonyms:
    3. CAS NO:54926-32-8
    4. Molecular Formula: C16H21NSi
    5. Molecular Weight: 255.435
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54926-32-8.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: Methanamine, N,N-dimethyl-1-(methyldiphenylsilyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methanamine, N,N-dimethyl-1-(methyldiphenylsilyl)-(54926-32-8)
    11. EPA Substance Registry System: Methanamine, N,N-dimethyl-1-(methyldiphenylsilyl)-(54926-32-8)
  • 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: 54926-32-8(Hazardous Substances Data)

54926-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54926-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,2 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54926-32:
(7*5)+(6*4)+(5*9)+(4*2)+(3*6)+(2*3)+(1*2)=138
138 % 10 = 8
So 54926-32-8 is a valid CAS Registry Number.

54926-32-8Relevant articles and documents

SYNTHESE UND REAKTIONSVERHALTEN VON (DIALKYLAMINOMETHYL)CHLORSILANEN UND -STANNANEN

Tzschach, A.,Uhlig, W.,Kellner, K.

, p. 17 - 24 (2007/10/02)

(Dialkylaminomethyl)chlorosilanes have been obtained by the reaction of trichlorosilane with bis(dimethylamino)methane.The corresponding stannanes have been prepared by the addition of methyleneimmonium halides to SnCl2.In the silicon compounds a covalent Si-CH2-N= bond is observed, while the tin compounds have ionic structures.Reactions of the new compounds are described.

Ylide Reactions of Benzyldimethylammonium Halides

Sato, Yoshiro,Yagi, Yoko,Koto, Masami

, p. 613 - 617 (2007/10/02)

Deprotonation of benzyldimethylammonium halides (10) with sodium amide or n-butyllithium afforded silylated ylide intermediates 11, which were rearranged into N,N-dimethyl-2-benzylamines (13) accompanied by the formation of Sommelet-Hauser and Stevens rearrangement products (12 and 22).The ylide formation by the cleavage of carbon-silicon bonds also is discussed in the reaction of 10 with sodium amide and lithium aluminum hydride.

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