6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE

Modify Date: 2024-01-14 16:11:10

6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE Structure
6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE structure
Common Name 6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE
CAS Number 2240-25-7 Molecular Weight 190.00
Density 1.3±0.1 g/cm3 Boiling Point 359.5±42.0 °C at 760 mmHg
Molecular Formula C4H4BrN3O Melting Point 240-243ºC
MSDS USA Flash Point 171.2±27.9 °C
Symbol GHS05 GHS07
GHS05, GHS07
Signal Word Danger

 Use of 6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE


4-Amino-5-bromopyrimidin-2(1H)-one is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 6-amino-5-bromo-1H-pyrimidin-2-one
Synonym More Synonyms

 6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE Biological Activity

Description 4-Amino-5-bromopyrimidin-2(1H)-one is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 359.5±42.0 °C at 760 mmHg
Melting Point 240-243ºC
Molecular Formula C4H4BrN3O
Molecular Weight 190.00
Flash Point 171.2±27.9 °C
Exact Mass 263.071320
PSA 72.03000
LogP 3.14
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.583
Water Solubility Soluble in formic acid (50 mg/ml).

 Safety Information

Symbol GHS05 GHS07
GHS05, GHS07
Signal Word Danger
Hazard Statements H302-H315-H317-H318-H335
Precautionary Statements P261-P280-P305 + P351 + P338
Hazard Codes Xn
Risk Phrases 22-37/38-41-43-48-20/21/22
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933599090

 Customs

HS Code 2933599090
Summary 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles15

More Articles
Structure-activity relationships of beta-D-(2S,5R)- and alpha-D-(2S,5S)-1,3-oxathiolanyl nucleosides as potential anti-HIV agents.

J. Med. Chem. 36(18) , 2627-38, (1993)

The beta-D-(2S,5R)- and alpha-D-(2S,5S)-1,3-oxathiolanylpyrimidine and -purine nucleosides with natural nucleoside configuration were synthesized and evaluated against HIV-1 in human peripheral blood ...

Formation of intrastrand cross-link products between cytosine and adenine from UV irradiation of d((Br)CA) and duplex DNA containing a 5-bromocytosine.

J. Am. Chem. Soc. 127(40) , 13969-77, (2005)

Here, we showed that Pyrex-filtered UV light irradiation of d((Br)CA) gave rise to three types of intrastrand cross-link products, that is, d(C[5-N6]A), d(C[5-2]A), and d(C[5-8]A), where the C5 carbon...

Lifetime regulation of the charge-separated state in DNA by modulating the oxidation potential of guanine in DNA through hydrogen bonding.

J. Am. Chem. Soc. 126(40) , 12843-6, (2004)

A series of naphthalimide (NI)- and 5-bromocytosine ((br)C)-modified oligodeoxynucleotides (ODNs) were prepared, and their lifetimes of the charge-separated states during the photosensitized one-elect...

 Synonyms

EINECS 218-806-8
1,4-Naphthalenedione, 2-chloro-3-[(2-methylpropyl)amino]-
5-bromoycytosine
4-Amino-5-bromo-2-hydroxypyrimidine
2-chloro-3-(isobutylamino)-1,4-dihydronaphthalene-1,4-dione
MFCD00056025
4-amino-5-bromopyrimidin-2-ol
5-Bromocytosine
bromocytosine
4-amino-5-bromo-1H-pyrimidin-2-one
6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE
2-Chloro-3-(isobutylamino)-1,4-naphthoquinone
F3096-1966