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19808-30-1

19808-30-1 Structure

19808-30-1 Structure
IdentificationBack Directory
[Name]

5-bromo-1H-pyrimidin-4-one
[CAS]

19808-30-1
[Synonyms]

Einecs 243-334-4
5-Bromo-4-Pyrimidone
5-Bromo-4(3H)-pyrimidone
5-BroMopyriMidin-4(3H)-one
5-bromo-1H-pyrimidin-6-one
5-BROMOPYRIMIDIN-4(1H)-ONE
5-Bromo-4(1H)-pyrimidinone
5-bromo-1H-pyrimidin-4-one
5-Bromopyrimidine-4(3H)-one
5-Bromo-4-hydroxypyrimidine
4(1H)-Pyrimidinone, 5-bromo-
4(3H)-Pyrimidinone, 5-bromo-
5-Bromopyrimidin-4(1H)-one,97%
5-bromo-3,4-dihydropyrimidin-4-one
5-Bromo-3,4-dihydropyrimidine-4-one
5-BroMo-4-hydroxypyriMidine.1/2H2SO4
5-bromo-1H-pyrimidin-4-one ISO 9001:2015 REACH
[EINECS(EC#)]

243-334-4
[Molecular Formula]

C4H3BrN2O
[MDL Number]

MFCD00223740
[MOL File]

19808-30-1.mol
[Molecular Weight]

174.983
Chemical PropertiesBack Directory
[Melting point ]

198-200℃
[density ]

2.00±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

7.25±0.40(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C4H3BrN2O/c5-3-1-6-2-7-4(3)8/h1-2H,(H,6,7,8)
[InChIKey]

CLJIGLPOBRSBNU-UHFFFAOYSA-N
[SMILES]

C1=NC=C(Br)C(=O)N1
[EPA Substance Registry System]

5-Bromo-4(1H)-pyrimidinone (19808-30-1)
Questions And AnswerBack Directory
[Uses]

5-Bromopyrimidine-4-one is a pyrimidine derivative and can be used as a pharmaceutical intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[TSCA ]

Yes
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

5-bromo-1H-pyrimidin-4-one(19808-30-1)MS
5-bromo-1H-pyrimidin-4-one(19808-30-1)1HNMR
5-bromo-1H-pyrimidin-4-one(19808-30-1)IR1
5-bromo-1H-pyrimidin-4-one(19808-30-1)IR2
Hazard InformationBack Directory
[Synthesis]

4-Pyrimidinol

51953-18-5

5-bromo-1H-pyrimidin-4-one

19808-30-1

Step A: Preparation of 5-bromopyrimidin-4(3H)-one: bromine (16.0 mL, 312 mmol) was slowly added dropwise to a suspension of chloroform (1 L) of 4-hydroxypyrimidine (30 g, 312 mmol) at 0 °C. Methanol (10 mL) was then added as a catalyst and the reaction mixture was stirred at 0 °C for 12 hours. Upon completion of the reaction, the resulting white solid product was collected by filtration, washed sequentially with hexane and ether, and then dried under vacuum to afford 5-bromopyrimidin-4-one (50 g, 91.5% yield). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 11.15 (broad single peak, 1H), 8.42 (single peak, 1H), 8.40 (single peak, 1H).

[References]

[1] Patent: US2007/238726, 2007, A1. Location in patent: Page/Page column 75
[2] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 16, p. 3905 - 3912
[3] Journal of the Chemical Society, 1955, p. 3478,3481
[4] Patent: WO2013/111105, 2013, A1. Location in patent: Page/Page column 125
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