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CAS

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447440-44-0

(3aR,7aR)-2-Allyl-1,3-dibenzyl-2-chloro-octahydro-benzo[1,3,2]diazasilole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 447440-44-0 Structure

  • Basic information

    1. Product Name: (3aR,7aR)-2-Allyl-1,3-dibenzyl-2-chloro-octahydro-benzo[1,3,2]diazasilole
    2. Synonyms: (3aR,7aR)-2-Allyl-1,3-dibenzyl-2-chloro-octahydro-benzo[1,3,2]diazasilole
    3. CAS NO:447440-44-0
    4. Molecular Formula:
    5. Molecular Weight: 397.035
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 447440-44-0.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: (3aR,7aR)-2-Allyl-1,3-dibenzyl-2-chloro-octahydro-benzo[1,3,2]diazasilole(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3aR,7aR)-2-Allyl-1,3-dibenzyl-2-chloro-octahydro-benzo[1,3,2]diazasilole(447440-44-0)
    11. EPA Substance Registry System: (3aR,7aR)-2-Allyl-1,3-dibenzyl-2-chloro-octahydro-benzo[1,3,2]diazasilole(447440-44-0)

  • 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: 447440-44-0(Hazardous Substances Data)

447440-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 447440-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,7,4,4 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 447440-44:
(8*4)+(7*4)+(6*7)+(5*4)+(4*4)+(3*0)+(2*4)+(1*4)=150
150 % 10 = 0
So 447440-44-0 is a valid CAS Registry Number.

447440-44-0Relevant articles and documents

Strained silacycles in organic synthesis: A new reagent for the enantioselective allylation of aldehydes

Kinnaird, James W. A.,Ng, Pui Yee,Kubota, Katsumi,Wang, Xiaolun,Leighton, James L.

, p. 7920 - 7921 (2002)

A new reagent for the enantioselective allylation of aliphatic aldehydes has been developed. The reagent is easily prepared in a single step from commercially available materials and may be stored without significant decomposition. The reactivity of the r

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