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3,N4-ETHENOCYTOSINE

Product Name
3,N4-ETHENOCYTOSINE
CAS No.
55662-66-3
Chemical Name
3,N4-ETHENOCYTOSINE
Synonyms
3,n(4)-ethanocytosine;imidazo[1,2-c]pyrimidin-5-ol;imidazo[1,2-f]pyrimidin-5-ol;IMidazo[1,2-c]pyriMidin-5(6H)-one
CBNumber
CB9503443
Molecular Formula
C6H5N3O
Formula Weight
135.12
MOL File
55662-66-3.mol
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3,N4-ETHENOCYTOSINE Property

Density 
1.51±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
7.09±0.20(Predicted)
Appearance
Light brown to brown Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Matrix Scientific
Product number
296256
Product name
Imidazo[1,2-c]pyrimidin-5(6H)-one
Packaging
100.00mg
Price
$32
Updated
2026/05/19
Matrix Scientific
Product number
296256
Product name
Imidazo[1,2-c]pyrimidin-5(6H)-one
Packaging
250.00mg
Price
$54
Updated
2026/05/19
Matrix Scientific
Product number
296256
Product name
Imidazo[1,2-c]pyrimidin-5(6H)-one
Packaging
1.00g
Price
$113
Updated
2026/05/19
Crysdot
Product number
CD11104848
Product name
Imidazo[1,2-c]pyrimidin-5(6H)-one
Purity
95+%
Packaging
250mg
Price
$232
Updated
2026/05/26
Crysdot
Product number
CD11104848
Product name
Imidazo[1,2-c]pyrimidin-5(6H)-one
Purity
95+%
Packaging
1g
Price
$579
Updated
2026/05/26
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3,N4-ETHENOCYTOSINE Chemical Properties,Usage,Production

Definition

ChEBI: 3,N(4)-ethenocytosine is an organic heterobicyclic compound. It has a role as a mutagen. It is functionally related to a cytosine. It derives from a hydride of an imidazo[1,2-c]pyrimidine.

Synthesis

107-20-0

71-30-7

55662-66-3

Procedure for the synthesis of imidazo[1,2-c]pyrimidin-5(6H)-one (13): 50% aqueous chloroacetaldehyde (0.686 mL, 5.40 mmol) was added to a stirred solution of 6-aminopyrimidin-2(1H)-one (500 mg, 4.50 mmol) in N,N-dimethylformamide (DMF, 10 mL). The reaction mixture was stirred at 70 °C for 16 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was washed with ethanol and ether to afford the target compound 13 as a light brown powder (320 mg, 53% yield). Thin layer chromatography (TLC) analysis showed Rf = 0.47 (unfolding agent: ethyl acetate/methanol, 4:1). The melting point of the product was 281-282 °C. Nuclear magnetic resonance hydrogen spectrum (1H NMR, 400 MHz, [D6]DMSO): δ = 6.62 (d, 1H, 3J = 7.6 Hz), 7.28 (d, 1H, 3J = 7.6 Hz), 7.41 (d, 1H, 3J = 1.2 Hz), 7.80 (d, 1H, 3J = 1.2 Hz), 11.6 (bs, 1H). Nuclear magnetic resonance carbon spectrum (13C NMR, 100 MHz, [D6]DMSO): δ = 97.7, 112.2, 129.4, 132.3, 145.9, 146.4. infrared spectrum (IR, KBr): ν = 3451, 3121, 3096, 1718, 1630, 1547, 1290, 1252, 1111 cm- 1. mass spectrum (ESI-MS): m/z 135.8 [M + H]+.

References

[1] Tetrahedron, 2014, vol. 71, # 1, p. 27 - 36
[2] Patent: WO2017/20944, 2017, A1. Location in patent: Page/Page column 16-17

3,N4-ETHENOCYTOSINE Preparation Products And Raw materials

Raw materials

Preparation Products

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3,N4-ETHENOCYTOSINE Suppliers

SynAsst Chemical.
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Energy Chemical
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