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(±)-2-(2-(1-methyl-2-oxoindolin-3-yl)ethyl)isoindoline-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101869-31-2 Structure
  • Basic information

    1. Product Name: (±)-2-(2-(1-methyl-2-oxoindolin-3-yl)ethyl)isoindoline-1,3-dione
    2. Synonyms: (±)-2-(2-(1-methyl-2-oxoindolin-3-yl)ethyl)isoindoline-1,3-dione
    3. CAS NO:101869-31-2
    4. Molecular Formula:
    5. Molecular Weight: 320.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101869-31-2.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: (±)-2-(2-(1-methyl-2-oxoindolin-3-yl)ethyl)isoindoline-1,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (±)-2-(2-(1-methyl-2-oxoindolin-3-yl)ethyl)isoindoline-1,3-dione(101869-31-2)
    11. EPA Substance Registry System: (±)-2-(2-(1-methyl-2-oxoindolin-3-yl)ethyl)isoindoline-1,3-dione(101869-31-2)
  • 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: 101869-31-2(Hazardous Substances Data)

101869-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101869-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,8,6 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 101869-31:
(8*1)+(7*0)+(6*1)+(5*8)+(4*6)+(3*9)+(2*3)+(1*1)=112
112 % 10 = 2
So 101869-31-2 is a valid CAS Registry Number.

101869-31-2Upstream product

101869-31-2Downstream Products

101869-31-2Relevant articles and documents

Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A

De, Subhadip,Das, Mrinal Kanti,Bhunia, Subhajit,Bisai, Alakesh

, p. 5922 - 5925 (2015)

The first enantioselective total syntheses of architecturally interesting prenylated pyrroloindole alkaloids, (-)-pseudophrynamines 272A (3d) and 270 (3b), have been achieved starting from enantioenriched 2-oxindoles having all-carbon quaternary stereocenters. A common strategy involving a thio-urea catalyzed aldol reaction is employed for the total synthesis of both spiro(pyrrolidinyl-oxindole) and hexahydropyrrolo[2,3-b]indole alkaloids.

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