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CAS

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132273-08-6

1,1,3,3-Tetramethyl-2-(1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,2,5]azadisilole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132273-08-6 Structure

  • Basic information

    1. Product Name: 1,1,3,3-Tetramethyl-2-(1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,2,5]azadisilole
    2. Synonyms: 1,1,3,3-Tetramethyl-2-(1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,2,5]azadisilole
    3. CAS NO:132273-08-6
    4. Molecular Formula:
    5. Molecular Weight: 311.574
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132273-08-6.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: 1,1,3,3-Tetramethyl-2-(1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,2,5]azadisilole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,3,3-Tetramethyl-2-(1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,2,5]azadisilole(132273-08-6)
    11. EPA Substance Registry System: 1,1,3,3-Tetramethyl-2-(1-phenyl-ethyl)-2,3-dihydro-1H-benzo[1,2,5]azadisilole(132273-08-6)

  • 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: 132273-08-6(Hazardous Substances Data)

132273-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132273-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,7 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132273-08:
(8*1)+(7*3)+(6*2)+(5*2)+(4*7)+(3*3)+(2*0)+(1*8)=96
96 % 10 = 6
So 132273-08-6 is a valid CAS Registry Number.

132273-08-6Downstream Products

132273-08-6Relevant articles and documents

The "benzostabase" protecting group for primary amines; application to aliphatic amines

Bonar-Law,Davis,Dorgan,Reetz,Wehrsig

, p. 6725 - 6728 (1990)

The "benzostabase" (BSB) protecting group has been applied to primary aliphatic amines. It can be introduced via a dehydrogenative silylation employing an air- and moisture-stable reagent, and is appreciably more acid-stable than the related "stabase" group. BSB protection has been used in a stereoselective synthesis of amino-alcohols involving the addition of organometallic reagents to protected amino-aldehydes under "non-chelation control".

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