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3-tert-butyl 1,1-dibenzyl 1-(1-oxoisoindolin-3-yl)propane-1,1,3-tricarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1383550-72-8 Structure
  • Basic information

    1. Product Name: 3-tert-butyl 1,1-dibenzyl 1-(1-oxoisoindolin-3-yl)propane-1,1,3-tricarboxylate
    2. Synonyms: 3-tert-butyl 1,1-dibenzyl 1-(1-oxoisoindolin-3-yl)propane-1,1,3-tricarboxylate
    3. CAS NO:1383550-72-8
    4. Molecular Formula:
    5. Molecular Weight: 543.617
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1383550-72-8.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: 3-tert-butyl 1,1-dibenzyl 1-(1-oxoisoindolin-3-yl)propane-1,1,3-tricarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-tert-butyl 1,1-dibenzyl 1-(1-oxoisoindolin-3-yl)propane-1,1,3-tricarboxylate(1383550-72-8)
    11. EPA Substance Registry System: 3-tert-butyl 1,1-dibenzyl 1-(1-oxoisoindolin-3-yl)propane-1,1,3-tricarboxylate(1383550-72-8)
  • 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: 1383550-72-8(Hazardous Substances Data)

1383550-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383550-72-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,5,5 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1383550-72:
(9*1)+(8*3)+(7*8)+(6*3)+(5*5)+(4*5)+(3*0)+(2*7)+(1*2)=168
168 % 10 = 8
So 1383550-72-8 is a valid CAS Registry Number.

1383550-72-8Downstream Products

1383550-72-8Relevant articles and documents

Electrochemically initiated tandem and sequential conjugate addition processes: One-pot synthesis of diverse functionalized isoindolinones

Antico, Pasqualmorica,Capaccio, Vito,Di Mola, Antonia,Massa, Antonio,Palombi, Laura

, p. 1717 - 1724 (2012)

A tandem aldol-heterocyclization-rearrangement reaction and one-pot sequential Michael addition allowed a direct access to highly functionalized 3-isoindolinones containing quaternary carbon centers. The desired products are obtained under mild conditions and in short reaction times by galvanostatic electrolysis in a divided cell. A further tandem intramolecular heterocyclization reaction leading to synthetically relevant hemiaminal derivatives has been established with suitable Michael acceptors. Copyright

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