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114738-94-2

(+/-)-2-<2,3,5,6,7,8-Hexahydro-1-<(4-methoxyphenyl)methylthio>-5-oxo-6-indolizinyl>-1H-isoindol-1,3(2H)-dion is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114738-94-2 Structure

  • Basic information

    1. Product Name: (+/-)-2-<2,3,5,6,7,8-Hexahydro-1-<(4-methoxyphenyl)methylthio>-5-oxo-6-indolizinyl>-1H-isoindol-1,3(2H)-dion
    2. Synonyms:
    3. CAS NO:114738-94-2
    4. Molecular Formula:
    5. Molecular Weight: 434.516
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114738-94-2.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-<2,3,5,6,7,8-Hexahydro-1-<(4-methoxyphenyl)methylthio>-5-oxo-6-indolizinyl>-1H-isoindol-1,3(2H)-dion(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-2-<2,3,5,6,7,8-Hexahydro-1-<(4-methoxyphenyl)methylthio>-5-oxo-6-indolizinyl>-1H-isoindol-1,3(2H)-dion(114738-94-2)
    11. EPA Substance Registry System: (+/-)-2-<2,3,5,6,7,8-Hexahydro-1-<(4-methoxyphenyl)methylthio>-5-oxo-6-indolizinyl>-1H-isoindol-1,3(2H)-dion(114738-94-2)

  • 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: 114738-94-2(Hazardous Substances Data)

114738-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114738-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,3 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 114738-94:
(8*1)+(7*1)+(6*4)+(5*7)+(4*3)+(3*8)+(2*9)+(1*4)=132
132 % 10 = 2
So 114738-94-2 is a valid CAS Registry Number.

114738-94-2Downstream Products

114738-94-2Relevant articles and documents

Diastereoselective Syntheses of rac-Slaframine and rac-6-epi-Slaframine

Dartmann, Mechthild,Flitsch, Wilhelm,Krebs, Bernt,Pandl, Klaus,Westfechtel, Alfred

, p. 695 - 704 (2007/10/02)

Indolizidinones 8 have been obtained from thalidomide (5) and cyclopropylphosphonium salts 6 in good yields.Acid-catalyzed rearrangement of 8a gave the isomer 11.A regio- and stereoselective acetoxylation of 8a and 11 was achieved with lead tetraacetate: using standard conditions, acetates 15 and 16 were obtained; in the presence of triethylamine, however, 8a has been transformed into the acetoxy derivative 17. rac-6-epi-Slaframine (4) and rac-slaframine (1) were obtained from acetates 16 and 17 on conventional routes.

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