ChemicalBook--->CAS DataBase List--->32779-38-7

32779-38-7

32779-38-7 Structure

32779-38-7 Structure
IdentificationBack Directory
[Name]

2-Chloro-5-iodopyrimidine
[CAS]

32779-38-7
[Synonyms]

2-Cloro-5-Iodopyrimidine
Pyrimidine,2-chloro-5-iodo-
2-Chloro-5-iodopyrimidine,95%
2-Chloro-5-iodopyrimidine ISO 9001:2015 REACH
[Molecular Formula]

C4H2ClIN2
[MDL Number]

MFCD06200210
[MOL File]

32779-38-7.mol
[Molecular Weight]

240.43
Chemical PropertiesBack Directory
[Melting point ]

133.0 to 137.0 °C
[Boiling point ]

318℃
[density ]

2.187
[Fp ]

146℃
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[form ]

powder to crystal
[pka]

-2.78±0.22(Predicted)
[color ]

White to Gray to Brown
[Sensitive ]

Light Sensitive
[InChI]

InChI=1S/C4H2ClIN2/c5-4-7-1-3(6)2-8-4/h1-2H
[InChIKey]

WSZRCNZXKKTLQE-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NC=C(I)C=N1
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

WGK 3
[HS Code ]

2933.59.8000
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2-Amino-5-iodopyrimidine-->tert-Butyl nitrite-->Acetonitrile-->Copper(II) chloride
[Preparation Products]

5-iodopyriMidine-2-carbonitrile-->2-Chloro-4-(4-fluoro-phenyl)-pyrimidine
Questions And AnswerBack Directory
[Description]

2-Chloro-5-iodopyrimidine is 2-Chloro-5-iodopyridine is a halo-substituted pyridine, and it is used in biology application as synthesis intermediate in the multi-step synthesis.

Hazard InformationBack Directory
[Uses]

In organic synthesis, 2-chloro-5-iodopyrimidine can be used to synthesize other compounds containing pyrimidine ring structures, and it can also be used in coordination chemistry, organic electronic devices and other fields.
[Synthesis]

2-AMINO-5-IODOPYRIMIDINE

1445-39-2

2-Chloro-5-iodopyrimidine

32779-38-7

Step A. Preparation of 2-chloro-5-iodopyrimidine To a stirred solution of 5-iodopyrimidin-2-amine (2.21 g, 10.0 mmol) in acetonitrile (20 mL) was sequentially added copper(II) chloride (2.02 g, 15 mmol) and tert-butyl nitrite (1.55 g, 15 mmol) at room temperature and under argon protection. The reaction mixture was transferred to an oil bath preheated to 60 °C and reacted under argon atmosphere. After completion of the reaction, the mixture was cooled to room temperature and diluted with the addition of ether (20 mL). The insoluble material was removed by filtration and the filtrate was concentrated under reduced pressure. The crude product was dissolved in a small amount of dichloromethane (about 2 mL) and purified by passing through an 80 g ISCO silica gel column using a 20 min gradient elution (0% to 100% ethyl acetate/hexane). 2-Chloro-5-iodopyrimidine (778 mg, 31% yield) was finally obtained as an off-white solid.1H NMR (400 MHz, CDCl3) δ 8.79 (s, 2H).

[References]

[1] Journal of Organic Chemistry, 2008, vol. 73, # 23, p. 9326 - 9333
[2] Patent: WO2010/9183, 2010, A1. Location in patent: Page/Page column 79
[3] Patent: US4248618, 1981, A
[4] Patent: WO2013/186692, 2013, A1. Location in patent: Page/Page column 62
Spectrum DetailBack Directory
[Spectrum Detail]

2-Chloro-5-iodopyrimidine(32779-38-7)1HNMR
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