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1-({2-nitrophenyl}sulfonyl)indoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 301355-05-5 Structure
  • Basic information

    1. Product Name: 1-({2-nitrophenyl}sulfonyl)indoline
    2. Synonyms: 1-({2-nitrophenyl}sulfonyl)indoline
    3. CAS NO:301355-05-5
    4. Molecular Formula: C14H12N2O4S
    5. Molecular Weight: 304.32108
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 301355-05-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-({2-nitrophenyl}sulfonyl)indoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-({2-nitrophenyl}sulfonyl)indoline(301355-05-5)
    11. EPA Substance Registry System: 1-({2-nitrophenyl}sulfonyl)indoline(301355-05-5)
  • 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: 301355-05-5(Hazardous Substances Data)

301355-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 301355-05-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,3,5 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 301355-05:
(8*3)+(7*0)+(6*1)+(5*3)+(4*5)+(3*5)+(2*0)+(1*5)=85
85 % 10 = 5
So 301355-05-5 is a valid CAS Registry Number.

301355-05-5Relevant articles and documents

NRF2 SMALL MOLECULE INHIBITORS FOR CANCER THERAPY

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Page/Page column 140; 141, (2014/09/29)

Small molecule inhibitors of Nrf2 and methods of their use are provided for treating or preventing a disease, disorder or condition associated with an Nrf2- regulated pathway. The compound can be administered as a single agent or can be administered to enhance the efficacy of a chemotherapeutic drug and/or radiation therapy.

Rearrangement of indolinesulfonamides to sulfones using polyphosphoric acid (PPA)

Raszka, Brian,McKee, James,Zanger, Murray

experimental part, p. 1837 - 1846 (2010/07/05)

Unlike other N-alkylsulfonanilides, indolinesulfonamides hydrolyze in 98% sulfuric acid. Recent work in this laboratory has shown that rearrangement can be achieved by using polyphosphoric acid. A series of substituted indolinesulfonamides has been prepar

Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): Efficient formation of products derived from aryl radicals

Mahesh, Mohan,Murphy, John A.,Lestrat, Franck,Wessel, Hans Peter

supporting information; experimental part, (2010/04/22)

Tetrakis(dimethylamino)ethylene (TDAE 1), has been exploited for the first time as a mild reagent for the reduction of arenediazonium salts to aryl radical intermediates through a single electron transfer (SET) pathway. Cyclization of the aryl radicals produced in this way led, in appropriate substrates, to syntheses of indolines and indoles. Cascade radical cyclizations of aryl radicals derived from arenediazonium salts are also reported. The relative ease of removal of the oxidized by-products of TDAE from the reaction mixture makes the methodology synthetically attractive.

A mild inter- and intramolecular amination of aryl halides with a combination of CuI and CsOAc

Kubo, Tetsuji,Katoh, Chiharu,Yamada, Ken,Okano, Kentaro,Tokuyama, Hidetoshi,Fukuyama, Tohru

supporting information; experimental part, p. 11230 - 11236 (2009/04/11)

A unique combination of CuI and CsOAc was found to catalyze aryl amination under mild conditions. The reaction takes place at room temperature or at 90 °C with broad functional group compatibility. The intramolecular reaction was able to form five-, six-, and seven-membered rings with various protecting groups on the nitrogen atom. The scope of the intermolecular amination, as well as its applications to unsymmetrical N,N′-dialkylated phenylenediamines, was investigated.

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