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2-(m-nitrophenylamino)nicotinic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 57978-48-0 Structure
  • Basic information

    1. Product Name: 2-(m-nitrophenylamino)nicotinic acid
    2. Synonyms: 2-(m-nitrophenylamino)nicotinic acid
    3. CAS NO:57978-48-0
    4. Molecular Formula:
    5. Molecular Weight: 259.221
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 57978-48-0.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-(m-nitrophenylamino)nicotinic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(m-nitrophenylamino)nicotinic acid(57978-48-0)
    11. EPA Substance Registry System: 2-(m-nitrophenylamino)nicotinic acid(57978-48-0)
  • 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: 57978-48-0(Hazardous Substances Data)

57978-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57978-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,7 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57978-48:
(7*5)+(6*7)+(5*9)+(4*7)+(3*8)+(2*4)+(1*8)=190
190 % 10 = 0
So 57978-48-0 is a valid CAS Registry Number.

57978-48-0Relevant articles and documents

Hypoxia-selective antitumor agents derived from 1,9-diazaanthracene

Monge,Narro,Martinez-Crespo,Lopez de Cerain,Hamilton,Barker

, p. 441 - 445 (1994)

The nitroacridine derivative 9-[3-(N,N-dimethylamino)propylamino]- 1-nitroacridine (nitracrine) is a potent hypoxia-selective cytotoxin for tumor cells in culture. Modifications of the acridine ring result in altered DNA binding properties. This has sugge

PDE4 INHIBITORS SELECTIVE FOR THE LONG FORM OF PDE4 FOR TREATING INFLAMMATION AND AVOIDING SIDE EFFECTS

-

Page/Page column 125, (2010/07/10)

The present invention relates to compounds which are inhibitors of phosphodiesterase-4 (PDE4) useful for the treatment and prevention of stroke, myocardial infarct, cardiovascular inflammatory diseases and disorders and central nervous system disorders, t

Optionally substituted pyrido[2,3-d]pyridine-2,4(1H,3H)-diones and pyrido[2,]pyrimidine-2(1H,3H)-ones

-

, (2011/03/17)

The present invention relates to optionally substituted pyrido[2,3-d]pyrimidine-2,4(1H,3H)-diones or optionally substituted pyrido[2,3-d]pyrimidine-2(1H,3H)-ones, i.e., compounds of Formula I: STR1 wherein: Y is --CH2 -- or --C(O)--; R1 is hydrogen or --(CH2)n --R7, wherein: R7 is aryl or heteroaryl, and n is 1 or 2, provided that when Y is --C(O)--, R7 is heteroaryl; and R2, R3, R4, R5 and R6 are hydrogen, or one is selected from lower alkyl, halo, carboxy, methoxycarbonyl, carbamoyl, methylcarbamoyl, di-methylcarbamoyl, methylcarbonyl, methylthio, methylsulfinyl, methylsulfonyl, hydroxymethyl, amino, trifluoromethyl, cyano or nitro; or R2, R3, R4 and R5 are independently selected from hydrogen, lower alkyl, nitro, chloro, fluoro, methoxycarbonyl or methylcarbonyl, provided at least one is hydrogen, and R6 is hydrogen; or a pharmaceutically acceptable ester, ether or salt thereof.

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