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

CAS No.
13162-26-0
Chemical Name:
2,4-Dichloro-6-methyl-5-nitropyrimidine
Synonyms
2,4-Dic;NSC 122005;2,4-Dichloro-6-Methyl-5-Nitro;Methyl 2,6-Dichloro-5-nitropyriMidine;2,4-dichlor-6-methyl-5-nitropyrimidin;4-Dichloro-6-Methyl-5-nitro-pyriMidine;2,4-dichloro-6-methyl-5-nitropyrimidin;2,6-DICHLORO-4-METHYL-5-NITROPYRIMIDINE;2,4-DICHLORO-5-NITRO-6-METHYLPYRIMIDINE;2,4-DICHLORO-6-METHYL-5-NITROPYRIMIDINE
CBNumber:
CB6320858
Molecular Formula:
C5H3Cl2N3O2
Molecular Weight:
208
MDL Number:
MFCD00023196
MOL File:
13162-26-0.mol
MSDS File:
SDS
Last updated:2025-10-28 16:00:23
Product description Number Pack Size Price
2,4-Dichloro-6-methyl-5-nitropyrimidine D435450 25g $150
2,4-Dichloro-6-methyl-5-nitropyrimidine D3531-25 5g $333
2,4-Dichloro-5-nitro-6-methylpyrimidine ND70435 250g $340
2,4-DICHLORO-6-METHYL-5-NITROPYRIMIDINE 95.00% HCH0017657 1G $410
2,4-DICHLORO-6-METHYL-5-NITROPYRIMIDINE 95.00% HCH0017657 2.5G $425
More product size

2,4-Dichloro-6-methyl-5-nitropyrimidine Properties

Melting point 52-54°C
Boiling point 135-136 °C(Press: 22 Torr)
Density 1.626±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka -5.30±0.39(Predicted)
color Pale Yellow to Light Beige
Stability Moisture Sensitive
InChI InChI=1S/C5H3Cl2N3O2/c1-2-3(10(11)12)4(6)9-5(7)8-2/h1H3
InChIKey NBCOZXBHPKSFSA-UHFFFAOYSA-N
SMILES C1(Cl)=NC(C)=C([N+]([O-])=O)C(Cl)=N1
CAS DataBase Reference 13162-26-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P261-P280-P305+P351+P338
Hazard Codes  Xi,Xn
Risk Statements  22-41-36/37/38
Safety Statements  26-39-36/37/39
HS Code  29335990

2,4-Dichloro-6-methyl-5-nitropyrimidine price More Price(31)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC D435450 2,4-Dichloro-6-methyl-5-nitropyrimidine 13162-26-0 25g $150 2021-12-16 Buy
Usbiological D3531-25 2,4-Dichloro-6-methyl-5-nitropyrimidine 13162-26-0 5g $333 2021-12-16 Buy
Biosynth Carbosynth ND70435 2,4-Dichloro-5-nitro-6-methylpyrimidine 13162-26-0 250g $340 2021-12-16 Buy
American Custom Chemicals Corporation HCH0017657 2,4-DICHLORO-6-METHYL-5-NITROPYRIMIDINE 95.00% 13162-26-0 1G $410 2021-12-16 Buy
American Custom Chemicals Corporation HCH0017657 2,4-DICHLORO-6-METHYL-5-NITROPYRIMIDINE 95.00% 13162-26-0 2.5G $425 2021-12-16 Buy
Product number Packaging Price Buy
D435450 25g $150 Buy
D3531-25 5g $333 Buy
ND70435 250g $340 Buy
HCH0017657 1G $410 Buy
HCH0017657 2.5G $425 Buy

2,4-Dichloro-6-methyl-5-nitropyrimidine Chemical Properties,Uses,Production

Chemical Properties

Yellow Crystalline Solid

Uses

A synthetic intermediate

Synthesis

5-Nitro-6-methyluracil

16632-21-6

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

13162-26-0

General procedure for the synthesis of 2,4-dichloro-5-nitro-6-methylpyrimidine from 2,4-dihydroxy-6-methyl-5-nitropyrimidine: 2,4-dihydroxy-6-methyl-5-nitropyrimidine (1 eq.) was dissolved in 17.54 mL of phosphoryl chloride, and 2.92 mL of N,N-dimethylaniline (1 eq.) was slowly added dropwise at room temperature. Subsequently, 8.04 μL of DMF (0.00445 eq.) was slowly added under reflux conditions and the reaction lasted for 8 hours. Upon completion of the reaction, the trichlorophosphorus oxide was removed by distillation under reduced pressure. Ice water was added to the residue and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was removed by rotary evaporation to give a light yellow to brown oil. The oily substance was purified by column chromatographic separation to give a final yellow solid 2,4-dichloro-5-nitro-6-methylpyrimidine (1 g) in 65% yield.

References

[1] Patent: CN105906621, 2016, A. Location in patent: Paragraph 0031
[2] Bulletin de la Societe Chimique de France, 1951, p. 428
[3] Helvetica Chimica Acta, 1951, vol. 34, p. 835,837
[4] Journal of the Chemical Society, 1951, p. 1004,1015
[5] Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, vol. 24, p. 84

16632-21-6
13162-26-0
Synthesis of 2,4-Dichloro-6-methyl-5-nitropyrimidine from 5-Nitro-6-methyluracil
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View Lastest Price from 2,4-Dichloro-6-methyl-5-nitropyrimidine manufacturers

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2,4-Dichloro-6-methyl-5-nitropyrimidine pictures 2026-02-28 2,4-Dichloro-6-methyl-5-nitropyrimidine
13162-26-0
US $0.00 / kg 1kg 98% Customise Hefei Lbao Physical & Chemical Science Co.,Ltd
2,4-Dichloro-6-methyl-5-nitropyrimidine  pictures 2025-11-18 2,4-Dichloro-6-methyl-5-nitropyrimidine
13162-26-0
US $1.10 / g 1g 99.00% 100 Tons Min Dideu Industries Group Limited
2,4-Dichloro-6-methyl-5-nitropyrimidine pictures 2023-06-19 2,4-Dichloro-6-methyl-5-nitropyrimidine
13162-26-0
US $0.00-0.00 / kg 1kg 98% Up to kgs Capot Chemical Co.,Ltd.

2,4-Dichloro-6-methyl-5-nitropyrimidine Spectrum

2,4-DICHLORO-6-METHYL-5-NITROPYRIMIDINE 2,4-DICHLORO-5-NITRO-6-METHYLPYRIMIDINE 2,6-DICHLORO-4-METHYL-5-NITROPYRIMIDINE 2,4-Dichloro-6-Methyl-5-Nitro Pyrimidine, 2,4-dichloro-6-methyl-5-nitro- 2,4-Dichloro-6-methyl-5-nitropyrimidine ,98% 2,4-dichloro-6-methyl-5-nitropyrimidin 4-Dichloro-6-Methyl-5-nitro-pyriMidine Methyl 2,6-Dichloro-5-nitropyriMidine NSC 122005 2,4-Dic 2,4-Dichloro-6-methyl-5-nitropyrimidine ISO 9001:2015 REACH 2,4-dichlor-6-methyl-5-nitropyrimidin 13162-26-0 13126-26-0 162-26-0 C5H4Cl2N3O2 C5H3Cl2N3O2 C5H3C12N3O2 Heterocycle-Pyrimidine series Bases & Related Reagents Nucleotides Pyrimidine Series Nucleotides and Nucleosides Pyrimidines APIs & Intermediate Pyrimidine Pyridines, Pyrimidines, Purines and Pteredines