ChemicalBook > CAS DataBase List > 3,N4-ETHENOCYTOSINE

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
More
Less

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
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
NUC0003911
Product name
3,N4-ETHENOCYTOSINE
Purity
95.00%
Packaging
5MG
Price
$505.07
Updated
2021/12/16
Crysdot
Product number
CD11104848
Product name
Imidazo[1,2-c]pyrimidin-5(6H)-one
Purity
95+%
Packaging
1g
Price
$579
Updated
2021/12/16
Ambeed
Product number
A123740
Product name
Imidazo[1,2-c]pyrimidin-5(6H)-one
Purity
95%
Packaging
100mg
Price
$43
Updated
2021/12/16
Ambeed
Product number
A123740
Product name
Imidazo[1,2-c]pyrimidin-5(6H)-one
Purity
95%
Packaging
250mg
Price
$60
Updated
2021/12/16
Chemenu
Product number
CM253640
Product name
Imidazo[1,2-c]pyrimidin-5(6H)-one
Purity
95+%
Packaging
100mg
Price
$84
Updated
2021/12/16
More
Less

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

More
Less

3,N4-ETHENOCYTOSINE Suppliers

SynAsst Chemical.
Tel
021-60343070
Fax
021-35122006
Country
China
ProdList
12740
Advantage
55
Mashilabs (Shanghai) Co.,Ltd.
Tel
19916721580
Fax
QQ:3154870176
Email
mafarm@126.com
Country
China
ProdList
4542
Advantage
58
Nanjing XiZe Biotechnology CO., Ltd.
Tel
025-58362220 0086-15250997978
Fax
025-58362220
Email
sale@njxizebio.com
Country
China
ProdList
4855
Advantage
55
Shanghai TuZhi Chemical Co., Ltd.
Tel
19542790274
Fax
QQ1456295541
Email
2119559397@qq.com
Country
China
ProdList
753
Advantage
50
Biokitchen
Tel
021-021-021-31663258 13795219287
Fax
021-31663258
Email
donghuanwen@126.com
Country
China
ProdList
8816
Advantage
58
Jiangsu aikang biomedical research and development co., LTD
Tel
025-58859352 13155353615
Email
qzhang@aikonchem.com
Country
China
ProdList
15525
Advantage
58
Shanghai Kaiwei Chemical Technology Co., Ltd.
Tel
021-58461859 15821823057
Email
service@aiviche.com
Country
China
ProdList
49312
Advantage
58
Birdo (Shanghai) Medical Technology Co., Ltd.
Tel
021-58099077-8041 18601625411
Email
sales@birdotech.com
Country
China
ProdList
9764
Advantage
58
Taizhou Nanfeng Pharmaceutical Research Institute
Tel
nanfengdrug@163.com; 18616377689
Email
nanfengdrug@163.com
Country
China
ProdList
20009
Advantage
58
Shanghai Sunmonth Technology Co., LTD
Tel
15216675652
Email
xuanyuelj@163.com
Country
China
ProdList
2864
Advantage
58