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2078-09-3

4-methyl-2-nitro-N-propylaniline is an organic compound with the chemical formula C10H14N2O2. It is a derivative of aniline, featuring a methyl group at the 4th carbon, a nitro group at the 2nd carbon, and a propyl group attached to the nitrogen atom. This yellow crystalline solid is soluble in organic solvents and has a melting point of approximately 52-54°C. It is primarily used as an intermediate in the synthesis of dyes, pharmaceuticals, and other chemical products. Due to its potential reactivity and the presence of a nitro group, it should be handled with care, as it may pose health risks and is sensitive to heat and friction.

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  • 2078-09-3 Structure

  • Basic information

    1. Product Name: 4-methyl-2-nitro-N-propylaniline
    2. Synonyms: 4-methyl-2-nitro-N-propylaniline
    3. CAS NO:2078-09-3
    4. Molecular Formula:
    5. Molecular Weight: 194.233
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2078-09-3.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: 4-methyl-2-nitro-N-propylaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methyl-2-nitro-N-propylaniline(2078-09-3)
    11. EPA Substance Registry System: 4-methyl-2-nitro-N-propylaniline(2078-09-3)

  • 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: 2078-09-3(Hazardous Substances Data)

2078-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2078-09-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,7 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2078-09:
(6*2)+(5*0)+(4*7)+(3*8)+(2*0)+(1*9)=73
73 % 10 = 3
So 2078-09-3 is a valid CAS Registry Number.

2078-09-3Relevant articles and documents

Oxidative coupling of N,N-Dialkylanilines using iodic acid and sodium nitrite

Huddar, Sameerana N.,Mahajan, Ulhas S.,Akamanchi, Krishnacharya G.

scheme or table, p. 808 - 809 (2011/01/07)

A new reagent system, a combination of iodic acid and sodium nitrite has been investigated for oxidative coupling of N,N-disubstituted anilines. A facile para-selective coupling occurs to give benzidines at room temperature in water as a solvent. A tentative mechanism is proposed with some supporting experiments.

Synthesis of some new 2-substituted-phenyl-1H-benzimidazole-5-carbonitriles and their potent activity against Candida species

G?ker, Hakan,Ku?, Canan,Boykin, David W.,Yildiz, Sulhiye,Altanlar, Nurten

, p. 2589 - 2596 (2007/10/03)

New 2-substituted-phenyl-1H-benzimidazole-5-carboxylic acids (35, 38), ethyl-5-carboxylate (36), -5-carboxamides (37, 39),-5-carboxaldehyde (42), -5-chloro (40), -5-trifluoromethyl (41), and -5-carbonitriles (44-53, 55-67), -6-carbonitrile (54) were prepa

A 'one-pot' phase transfer alkylation/hydrolysis of o-nitrotrifluoroacetanilides. A convenient route to N-alkyl o-phenylenediamines

Brown, Samuel A.,Rizzo, Carmelo J.

, p. 4065 - 4080 (2007/10/03)

A variety of o-nitrotrifluoroacetanilides undergo a one-pot alkylation/hydrolysis to give N-alkyl o-nitroanilines in 40-94% yield. Dimethylsulfate, benzyl bromide and 1-bromo-propane were used as the electrophiles.

Synthesis of 1-Alkoxy-2-Alkyl-Benzimidazoles from 2-Nitroanilines via Tandem N-Alkylation-Cyclization-O-Alkylation

Gardiner, John M.,Loyns, Colin R.,Schwalbe, Carl H.,Barrett, Garry C.,Lowe, Philip R.

, p. 4101 - 4110 (2007/10/02)

Substituted 2-nitroanilines react with benzylic, allyl and alkyl halides to give 2-aryl-1-benzyloxy-, 1-allyloxy-2-vinyl- and 1-alkoxy-2-alkyl-benzimidazoles, in a one-pot cascade process involving 1-alkylation-cyclization-O-alkylation. 2-Aryl-1-benzyloxy- and 1-allyloxy-2-vinyl- derivatives are obtained in high yields (79-98percent), while with simple alkyl halides, yields of the benzimidazoles are substrate dependent.An X-ray crystal structure of 2,4-dimethyl-1-ethoxybenzimidazole is presented.

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