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2,6-Dichloropyrimidine-4-carbonyl chloride

CAS No.
26830-94-4
Chemical Name:
2,6-Dichloropyrimidine-4-carbonyl chloride
Synonyms
2,4-Dichloropyrimidine-6-carbonyl chloride;4-Pyrimidinecarbonyl chloride, 2,6-dichloro-
CBNumber:
CB51489982
Molecular Formula:
C5HCl3N2O
Molecular Weight:
211.43
MDL Number:
MFCD08444236
MOL File:
26830-94-4.mol
Last updated:2026-09-12 18:53:12

2,6-Dichloropyrimidine-4-carbonyl chloride Properties

Density 1.675
refractive index 1.588

SAFETY

Risk and Safety Statements

2,6-Dichloropyrimidine-4-carbonyl chloride price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth BBA83094 2,6-Dichloropyrimidine-4-carbonyl chloride 26830-94-4 2.5g $468.75 2026-06-04 Buy
aablocks AA00BII9 2,6-Dichloropyrimidine-4-carbonyl chloride 95% 26830-94-4 100mg $16 2026-05-28 Buy
aablocks AA00BII9 2,6-Dichloropyrimidine-4-carbonyl chloride 95% 26830-94-4 250mg $21 2026-05-28 Buy
aablocks AA00BII9 2,6-Dichloropyrimidine-4-carbonyl chloride 95% 26830-94-4 1g $56 2026-05-28 Buy
Crysdot CD11155941 2,6-Dichloropyrimidine-4-carbonyl chloride 95+% 26830-94-4 1g $108 2026-05-26 Buy
Product number Packaging Price Buy
BBA83094 2.5g $468.75 Buy
AA00BII9 100mg $16 Buy
AA00BII9 250mg $21 Buy
AA00BII9 1g $56 Buy
CD11155941 1g $108 Buy

2,6-Dichloropyrimidine-4-carbonyl chloride Chemical Properties, Uses, Production

Uses

2,6-Dichloropyrimidine-4-carbonyl Chloride,

Synthesis

Orotic acid

65-86-1

2,6-DICHLOROPYRIMIDINE-4-CARBONYL CHLORIDE

26830-94-4

General procedure for the synthesis of 2,6-dichloropyrimidine-4-carbonyl chloride from orotate monohydrate: 1. In a dry reaction flask, whey acid monohydrate (34.828 g, 200.0 mmol), phosphorus trichloride (100 mL, 1092 mmol) and N,N-dimethylformamide (20 drops) were added. 2. The reaction mixture was heated to 110 °C and the reaction was stirred at this temperature overnight. 3. After completion of the reaction, the mixture was cooled to room temperature. 4. Hexane (500 mL) was added to the cooled dark reaction mixture with vigorous stirring. 5. Separate the hexane layer and wash rapidly with deionized water (100 mL x 1) and saturated saline (100 mL x 1) in that order. 6. Dry the organic phase with anhydrous magnesium sulfate and filter to remove the desiccant. 7. The solvent was carefully evaporated under reduced pressure to afford 2,6-dichloropyrimidine-4-carbonyl chloride as a light yellow liquid (26.13 g, 123.6 mmol, 62% yield). Product characterization: 1H NMR (400 MHz, CDCl3) δ 7.93 (s, 1H).

References

[1] Patent: WO2013/30665, 2013, A1. Location in patent: Page/Page column 104; 105
[2] Patent: WO2013/72758, 2013, A1. Location in patent: Page/Page column 93
[3] Patent: WO2014/135955, 2014, A1. Location in patent: Paragraph 0311
[4] Patent: WO2015/31036, 2015, A1. Location in patent: Page/Page column 72; 73
[5] Patent: US2015/175569, 2015, A1. Location in patent: Paragraph 0321

2,6-Dichloropyrimidine-4-carbonyl chloride Preparation Products And Raw materials

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4-Pyrimidinecarbonyl chloride, 2,6-dichloro- 2,4-Dichloropyrimidine-6-carbonyl chloride 26830-94-4