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CAS

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1578230-39-3

(S)-methyl 2-(5-nitro-2,3-dioxoindolin-1-yl)-4-oxo-4-phenylbutanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1578230-39-3 Structure

  • Basic information

    1. Product Name: (S)-methyl 2-(5-nitro-2,3-dioxoindolin-1-yl)-4-oxo-4-phenylbutanoate
    2. Synonyms: (S)-methyl 2-(5-nitro-2,3-dioxoindolin-1-yl)-4-oxo-4-phenylbutanoate
    3. CAS NO:1578230-39-3
    4. Molecular Formula:
    5. Molecular Weight: 382.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1578230-39-3.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: (S)-methyl 2-(5-nitro-2,3-dioxoindolin-1-yl)-4-oxo-4-phenylbutanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-methyl 2-(5-nitro-2,3-dioxoindolin-1-yl)-4-oxo-4-phenylbutanoate(1578230-39-3)
    11. EPA Substance Registry System: (S)-methyl 2-(5-nitro-2,3-dioxoindolin-1-yl)-4-oxo-4-phenylbutanoate(1578230-39-3)

  • 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: 1578230-39-3(Hazardous Substances Data)

1578230-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1578230-39-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,8,2,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1578230-39:
(9*1)+(8*5)+(7*7)+(6*8)+(5*2)+(4*3)+(3*0)+(2*3)+(1*9)=183
183 % 10 = 3
So 1578230-39-3 is a valid CAS Registry Number.

1578230-39-3Upstream product

1578230-39-3Downstream Products

1578230-39-3Relevant articles and documents

Remote activation of the nucleophilicity of isatin

Zari, Sergei,Kudrjashova, Marina,Pehk, Tonis,Lopp, Margus,Kanger, Tonis

, p. 1740 - 1743 (2014)

The concept of the remote activation of reactivity was first applied in asymmetric organocatalysis. An isatin 3-phenylimine derivative acts as a donor in the thiourea catalyzed asymmetric addition to unsaturated 1,4-ketoesters, affording aza-Michael adducts in high enantiomeric purity and yield.

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