Cas no 13162-26-0 (2,4-Dichloro-6-methyl-5-nitropyrimidine)

2,4-Dichloro-6-methyl-5-nitropyrimidine structure
13162-26-0 structure
Product Name:2,4-Dichloro-6-methyl-5-nitropyrimidine
CAS No:13162-26-0
MF:C5H3Cl2N3O2
MW:208.002218484879
MDL:MFCD00023196
CID:49069
PubChem ID:275294
Update Time:2025-04-18

2,4-Dichloro-6-methyl-5-nitropyrimidine Chemical and Physical Properties

Names and Identifiers

    • 2,4-Dichloro-6-methyl-5-nitropyrimidine
    • 2,4-Dichloro-5-nitro-6-methylpyrimidine
    • 2,4-Dichloro-6-Methyl-5-Nitro
    • Pyrimidine, 2,4-dichloro-6-methyl-5-nitro-
    • 2,6-DICHLORO-4-METHYL-5-NITROPYRIMIDINE
    • 2,4,5-TRIBROMOIMIDAZOLE
    • 2,4-dichlor-6-methyl-5-nitropyrimidin
    • 2,4-dichloro-5-methyl-5-nitropyrimidine
    • 2,6-dichloro-3-methyl-5-nitropyrimidine
    • 5-nitro-6-methyl-2,4-dichloropyrimidine
    • Methyl 2,6-dichloro-5-nitropyrimidine
    • NSC 122005
    • 4-Dichloro-6-Methyl-5-nitro-pyriMidine
    • 2,4-dichloro-6-methyl-5-nitropyrimidin
    • 2,4-Dichloro-6-methyl-5-nitropyrimidine ,98%
    • 2,4-Dichloro-6-methyl-5-nitro-pyrimidine
    • A2751
    • 2,4-Dichloro-6-methyl-5-nitro pyrimidine
    • 2,4dichloro-6-methyl-5-nitropyrimidine
    • 2,4-Dichloro-6-methyl-5-nitropyrimidine, AldrichCPR
    • AM20080229
    • AS-11858
    • FT-0636821
    • EN300-105048
    • GEO-03671
    • NSC-122005
    • SB60516
    • W-201054
    • A901022
    • CS-D1701
    • CHEMBL162141
    • SCHEMBL56358
    • 13162-26-0
    • AC-5941
    • SY017837
    • NBCOZXBHPKSFSA-UHFFFAOYSA-N
    • DTXSID10298254
    • MFCD00023196
    • NSC122005
    • AKOS002662660
    • STL115585
    • DB-216690
    • DB-015913
    • AG-690/08505042
    • MDL: MFCD00023196
    • Inchi: 1S/C5H3Cl2N3O2/c1-2-3(10(11)12)4(6)9-5(7)8-2/h1H3
    • InChI Key: NBCOZXBHPKSFSA-UHFFFAOYSA-N
    • SMILES: ClC1=C(C(C)=NC(=N1)Cl)[N+](=O)[O-]

Computed Properties

  • Exact Mass: 206.96000
  • Monoisotopic Mass: 206.96
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 0
  • Complexity: 186
  • 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
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 2.4
  • Topological Polar Surface Area: 71.6A^2

Experimental Properties

  • Color/Form: Pale-yellow to Yellow-brown Solid
  • Density: 1.626
  • Melting Point: 52-56°C
  • Boiling Point: 311.8℃ at 760 mmHg
  • Flash Point: 142.4 °C
  • Refractive Index: 1.597
  • Stability/Shelf Life: Moisture Sensitive
  • PSA: 71.60000
  • LogP: 2.52320

2,4-Dichloro-6-methyl-5-nitropyrimidine Security Information

2,4-Dichloro-6-methyl-5-nitropyrimidine Customs Data

  • HS CODE:2933599090
  • Customs Data:

    China Customs Code:

    2933599090

    Overview:

    2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the 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:

    2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

2,4-Dichloro-6-methyl-5-nitropyrimidine Pricemore >>

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2,4-Dichloro-6-methyl-5-nitropyrimidine Production Method

2,4-Dichloro-6-methyl-5-nitropyrimidine Related Literature

  • 1. Heterocyclic studies. Part XVI. Imidazo- and di-imidazo-pyrimidines
    Jim Clark,T. Ramsden J. Chem. Soc. C 1971 675
  • 2. Heterocyclic studies. Part XVII. Some 2,3-dihydroimidazo-[1,2-a]- and [1,2-c]-pyrimidines
    Jim Clark,T. Ramsden J. Chem. Soc. C 1971 679
  • 3. 1 : 2 : 4 : 6-Tetra-azaindenes and 1 : 4 : 6-triazaindan-2-ones from 5-aminopyrimidines
  • 4. 846. Glyoxalinopyrimidines. The cyclisation of some 4-2′-chloroethylaminopyrimidines
    G. R. Ramage,G. Trappe J. Chem. Soc. 1952 4410
  • 5. 224. An experimental study of some potentially tautomeric 2- and 4(6)-substituted pyrimidines
    J. R. Marshall,James Walker J. Chem. Soc. 1951 1004
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