Cas no 21203-55-4 (2,4,6-Trimethyl-3-nitropyridine)

2,4,6-Trimethyl-3-nitropyridine structure
21203-55-4 structure
Product Name:2,4,6-Trimethyl-3-nitropyridine
CAS No:21203-55-4
MF:C8H10N2O2
MW:166.177201747894
MDL:MFCD00110819
CID:51741
PubChem ID:2747698
Update Time:2025-04-18

2,4,6-Trimethyl-3-nitropyridine Chemical and Physical Properties

Names and Identifiers

    • 2,4,6-Trimethyl-3-nitropyridine
    • 2,4,6-Trimethyl-3-nitro-pyridin
    • 2,4,6-trimethyl-3-nitro-pyridine
    • 3-Nitro-2,4,6-collidin
    • 3-nitro-2,4,6-collidine
    • 3-nitro-2,4,6-trimethylpyridine
    • 3-Nitro-collidin
    • 3-Nitro-s-kollidin
    • AC-3558
    • SCHEMBL8033158
    • LS-07279
    • 2, 4, 6-trimethyl-3-nitropyridine
    • SB54094
    • Oprea1_155193
    • UQBHNBZGFVDCAH-UHFFFAOYSA-N
    • MixCom1_000152
    • MFCD00110819
    • DTXSID10372684
    • 2.4.6-TRIMETHYL-3-NITROPYRIDINE
    • CS-0316346
    • Maybridge1_000086
    • D96328
    • AKOS003342592
    • FT-0760433
    • 21203-55-4
    • A815195
    • AMY2369
    • ALBB-023236
    • Pyridine, 2,4,6-trimethyl-3-nitro-
    • DB-019842
    • MDL： MFCD00110819
    • Inchi： 1S/C8H10N2O2/c1-5-4-6(2)9-7(3)8(5)10(11)12/h4H,1-3H3
    • InChI Key： UQBHNBZGFVDCAH-UHFFFAOYSA-N
    • SMILES： [O-][N+](C1C(C)=NC(C)=CC=1C)=O

Computed Properties

  • Exact Mass: 166.07400
  • Monoisotopic Mass: 166.074227566g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 0
  • Complexity: 178
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.8
  • Topological Polar Surface Area: 58.7?2

Experimental Properties

  • PSA: 58.71000
  • LogP: 2.43820

2,4,6-Trimethyl-3-nitropyridine Customs Data

  • HS CODE：2933399090
  • Customs Data：

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

2,4,6-Trimethyl-3-nitropyridine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A029186549-1g
2,4,6-Trimethyl-3-nitropyridine
 21203-55-4 95%
1g
 $400.00 2023-09-02
TRC
T219540-250mg
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 21203-55-4
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Chemenu
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Chemenu
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eNovation Chemicals LLC
Y1055830-5g
2,4,6-Trimethyl-3-nitropyridine
 21203-55-4 95%
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abcr
AB414035-500 mg
2,4,6-Trimethyl-3-nitropyridine
 21203-55-4
500MG
 €254.60 2023-01-21
abcr
AB414035-1 g
2,4,6-Trimethyl-3-nitropyridine
 21203-55-4
1g
 €322.50 2023-06-16
abcr
AB414035-500mg
2,4,6-Trimethyl-3-nitropyridine; .
 21203-55-4
500mg
 €269.00 2025-04-20

2,4,6-Trimethyl-3-nitropyridine Related Literature

  • 1. The mechanism of the electrophilic substitution of heteroaromatic compounds. Part VI. The nitration of pyridines in the 3-position as free bases and as conjugate acids
    C. D. Johnson,A. R. Katritzky,B. J. Ridgewell,M. Viney J. Chem. Soc. B 1967 1204
  • 2. The mechanism of the electrophilic substitution of heteroaromatic compounds. Part VIII. The α-, β-, and γ-nitration of pyridine 1-oxides
    C. D. Johnson,A. R. Katritzky,Naeem Shakir,M. Viney J. Chem. Soc. B 1967 1213
  • 3. Notes
    G. L. Esteban,J. A. Kerr,A. F. Trotman-Dickenson,S. Gronowitz,A. R. Katritzky,R. E. Reavill,B. J. Ridgewell,M. Green,R. F. Hudson,J. S. Brimacombe,M. J. How,R. M. Acheson,G. R. Miller,A. O. Plunkett,R. G. Cavell,H. C. Clark,J. H. Holloway,R. D. Peacock,E. A. V. Ebsworth,M. J. Mays,B. O. Handford,W. B. Whalley,M. F. Grundon,B. E. Reynolds,A. A. R. Sayigh,Henri Ulrich,J. Rubinfeld,P. J. Palmer,B. L. Hollingsworth,D. G. Tuck,R. W. Bott,C. Eaborn,T. Hashimoto,J. Cymerman Craig,M. Moyle,B. K. Tidd,H. R. Arthur,W. D. Ollis,N. N. Greenwood,M. G. H. Wallbridge,K. W. Bentley,S. F. Dyke,A. R. Marshall,E. E. Smith,W. J. Whelan,P. A. Finan,M. T. Ahmed,A. J. Swallow J. Chem. Soc. 1963 3879

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