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4-CHLORO-2,6-DIPHENYLPYRIMIDINE

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Products Intro: Product Name:4-CHLORO-2,6-DIPHENYLPYRIMIDINE
CAS:29509-91-9
Purity:99%, 99.5% Sublimated Package:1KG;200USD|100KG;1USD
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Products Intro: Product Name:4-chloro-2,6-diphenylpyrimidine
CAS:29509-91-9
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Products Intro: Product Name:4-Chloro-2,6-diphenylpyrimidine
CAS:29509-91-9
Purity:99% Package:1KG,5KG,10KG
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CAS:29509-91-9
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G

4-CHLORO-2,6-DIPHENYLPYRIMIDINE manufacturers

  • 4-CHLORO-2,6-DIPHENYLPYRIMIDINE
  • 4-CHLORO-2,6-DIPHENYLPYRIMIDINE pictures
  • $200.00 / 1KG
  • 2025-09-25
  • CAS:29509-91-9
  • Min. Order: 1KG
  • Purity: 99%, 99.5% Sublimated
  • Supply Ability: g-kg-tons, free sample is available
4-CHLORO-2,6-DIPHENYLPYRIMIDINE Basic information
Product Name:4-CHLORO-2,6-DIPHENYLPYRIMIDINE
Synonyms:4-CHLORO-2,6-DIPHENYLPYRIMIDINE;6-CHLORO-2,4-DIPHENYLPYRIMIDINE;Pyrimidine, 4-chloro-2,6-diphenyl-;4-CDPP;2,6-diphenylpyrimidine-4-chloride;4-CHLORO-2,6-DIPHENYLPYRIMIDINE ISO 9001:2015 REACH
CAS:29509-91-9
MF:C16H11ClN2
MW:266.72
EINECS:
Product Categories:pyrimidine
Mol File:29509-91-9.mol
4-CHLORO-2,6-DIPHENYLPYRIMIDINE Structure
4-CHLORO-2,6-DIPHENYLPYRIMIDINE Chemical Properties
Melting point 104-105℃
Boiling point 339.2±35.0 °C(Predicted)
density 1.221
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka-0.99±0.30(Predicted)
form powder to crystal
color White to Almost white
Safety Information
HS Code 2933.59.8000
MSDS Information
4-CHLORO-2,6-DIPHENYLPYRIMIDINE Usage And Synthesis
Chemical PropertiesWhite solid
Synthesis Reference(s)Journal of Medicinal Chemistry, 47, p. 6529, 2004 DOI: 10.1021/jm049448r
Synthesis
2,4,6-Trichloropyrimidine

3764-01-0

(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZENE

24388-23-6

4-CHLORO-2,6-DIPHENYLPYRIMIDINE

29509-91-9

Using 2,4,6-trichloropyrimidine (10 g, 54.5 mmol) and (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene (22.3 g, 109 mmol) as raw material, catalyzed by tetrakis(triphenylphosphine)palladium (3.8 g, 3.27 mmol) in a mixed solvent of THF (240 mL) and water (120 mL). Potassium carbonate (45.2 g) was added and the reaction was stirred at 90 °C. Upon completion of the reaction, extraction was carried out with dichloromethane and water. The organic layer was dried with anhydrous magnesium sulfate and concentrated. Purified by silica gel column chromatography and recrystallization, 9.5 g of 4-chloro-2,6-diphenylpyrimidine was obtained in 65% yield.

References[1] Patent: KR2017/127593, 2017, A. Location in patent: Paragraph 0400-0402
[2] Patent: KR2017/120233, 2017, A. Location in patent: Paragraph 0511; 0512
[3] Patent: US2018/251473, 2018, A1. Location in patent: Paragraph 0253; 0254
[4] Patent: US2018/282276, 2018, A1. Location in patent: Paragraph 0222; 0223
Tag:4-CHLORO-2,6-DIPHENYLPYRIMIDINE(29509-91-9) Related Product Information
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