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113001-14-2

2-Quinoxalinamine, 3-(2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113001-14-2 Structure

  • Basic information

    1. Product Name: 2-Quinoxalinamine, 3-(2-nitrophenyl)-
    2. Synonyms:
    3. CAS NO:113001-14-2
    4. Molecular Formula: C14H10N4O2
    5. Molecular Weight: 266.259
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113001-14-2.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-Quinoxalinamine, 3-(2-nitrophenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Quinoxalinamine, 3-(2-nitrophenyl)-(113001-14-2)
    11. EPA Substance Registry System: 2-Quinoxalinamine, 3-(2-nitrophenyl)-(113001-14-2)

  • 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: 113001-14-2(Hazardous Substances Data)

113001-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113001-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,0 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113001-14:
(8*1)+(7*1)+(6*3)+(5*0)+(4*0)+(3*1)+(2*1)+(1*4)=42
42 % 10 = 2
So 113001-14-2 is a valid CAS Registry Number.

113001-14-2Downstream Products

113001-14-2Relevant articles and documents

Quinoxalino[2,3- c ]cinnolines and their 5- N -oxide: Alkoxylation of methyl-substituted quinoxalino[2,3- c ]cinnolines to acetals and orthoesters

Haddadin, Makhluf J.,El-Khatib, Mirna,Shoker, Tharallah A.,Beavers, Christine M.,Olmstead, Marilyn M.,Fettinger, James C.,Farber, Kelli M.,Kurth, Mark J.

, p. 8421 - 8427 (2011/12/14)

We report the alkoxylation of methyl-substituted quinoxalino[2,3-c] cinnolines to give acetals and orthoesters in high yields. Routes to the precursors of this alkoxylation reaction as well as other quinoxalino[2,3-c] cinnoline and their 5-oxide derivativ

o-Nitrobenzylidene Compounds. Part 4. The Cyanide-induced Cyclisation of o-Acetamido-N-(o-nitrobenzylidene)anilines: an Improved Route to Quinoxalinocinnolines

Shepherd, Thomas,Smith, David M.

, p. 501 - 506 (2007/10/02)

Cyclisation of o-acetamido-N-(o-nitrobenzylidene)anilines (7) with potassium cyanide in methanol (preferably under nitrogen) leads in most cases to quinoxalinocinnolines (6) of unambiguous substitution pattern.In some cases, cyclisation appears to be incomplete, and 2-amino-3-(o-nitrophenyl)quinoxalines (11) are obtained as by-products; in certain cases quinoxalinocinnoline 5-oxides (10) are also detected.These by-products are assumed to result from oxidation of intermediates in the cyclisation process (7) ----> (6).

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