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209115-59-3

N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 209115-59-3 Structure

  • Basic information

    1. Product Name: N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide
    2. Synonyms: N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide
    3. CAS NO:209115-59-3
    4. Molecular Formula:
    5. Molecular Weight: 402.471
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 209115-59-3.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: N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide(209115-59-3)
    11. EPA Substance Registry System: N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide(209115-59-3)

  • 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: 209115-59-3(Hazardous Substances Data)

209115-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209115-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,1,1 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 209115-59:
(8*2)+(7*0)+(6*9)+(5*1)+(4*1)+(3*5)+(2*5)+(1*9)=113
113 % 10 = 3
So 209115-59-3 is a valid CAS Registry Number.

209115-59-3Relevant articles and documents

The synthesis and in vitro cytotoxic studies of novel oxa-spermidine derivatives and homologues

Kuksa, Vladimir A.,Pavlov, Valentin A.,Lin, Paul Kong Thoo

, p. 1265 - 1267 (2007/10/03)

A series of oxa-spermidine derivatives and homologues were prepared and their anticancer properties were evaluated. All these compounds showed an average GI50 value in the range of 3.9-28.9 μM. SAR studies showed that the presence of a sulphonamido functionality and the length of the alkyl chain are important factors for an enhanced activity. (C) 2000 Elsevier Science Ltd. All rights reserved.

The Synthesis of Oxa-Analogues and Homologues of Naturally Occuring Polyamines

Lin, P. Kong Thoo,Kuksa, V. A.,Maguire, N. M.

, p. 859 - 866 (2007/10/03)

A number of polyamine oxa-analogues 14a-d, 19 have been synthesized.Spermidine oxa-analogues and homologues 14 were made from N-(aminooxypropyl)phthalimide 8a which was obtained either from the Fmoc-deprotection of N-phthalimide 4a or from the reaction between 3-bromopropylamine and N-hydroxyphthalimide, both reactions involving an unusual rearrangement mechanism.Sulphonated derivatives 9, 16, upon Mitsunobu condensation with N-protected 3-aminopropanol or N-alkylation with N-(bromoalkyl)phthalimides, afforded the fully protected spermidine and spermine oxa-analogues.Subsequent sequential deprotection gave spermidine analogues 14.Using the same strategy, spermine oxa-analogues 19 was synthesised. - Keywords: polyamines; oxa-analogues of polyamines; polyamine homologues; rearrangement; synthesis

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