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(2S,3aR,4S,8aR,8bS)-4-((dimethyl(phenyl)silyl)methyl)-2-phenylhexahydro-[1,3]dioxolo[4,5-a]pyrrolizin-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1431853-29-0 Structure
  • Basic information

    1. Product Name: (2S,3aR,4S,8aR,8bS)-4-((dimethyl(phenyl)silyl)methyl)-2-phenylhexahydro-[1,3]dioxolo[4,5-a]pyrrolizin-6-one
    2. Synonyms:
    3. CAS NO:1431853-29-0
    4. Molecular Formula:
    5. Molecular Weight: 393.558
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1431853-29-0.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: (2S,3aR,4S,8aR,8bS)-4-((dimethyl(phenyl)silyl)methyl)-2-phenylhexahydro-[1,3]dioxolo[4,5-a]pyrrolizin-6-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3aR,4S,8aR,8bS)-4-((dimethyl(phenyl)silyl)methyl)-2-phenylhexahydro-[1,3]dioxolo[4,5-a]pyrrolizin-6-one(1431853-29-0)
    11. EPA Substance Registry System: (2S,3aR,4S,8aR,8bS)-4-((dimethyl(phenyl)silyl)methyl)-2-phenylhexahydro-[1,3]dioxolo[4,5-a]pyrrolizin-6-one(1431853-29-0)
  • 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: 1431853-29-0(Hazardous Substances Data)

1431853-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1431853-29-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,1,8,5 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1431853-29:
(9*1)+(8*4)+(7*3)+(6*1)+(5*8)+(4*5)+(3*3)+(2*2)+(1*9)=150
150 % 10 = 0
So 1431853-29-0 is a valid CAS Registry Number.

1431853-29-0Relevant articles and documents

Asymmetric approach to hyacinthacines B1 and B2

Reddy, Paidi Venkatram,Smith, Julien,Kamath, Anushree,Jamet, Hélène,Veyron, Ama?l,Koos, Peter,Philouze, Christian,Greene, Andrew E.,Delair, Philippe

, p. 4840 - 4849 (2013/07/05)

Naturally occurring hyacinthacines B1 and B2 have been prepared from a common, easily available, advanced intermediate. The approach features several highly stereoselective transformations: inter alia, a dichloroketene-enol ether [2 + 2] cycloaddition, a Bruylants alkylation, and an amino-nitrile alkylation-reduction.

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