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

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

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	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.

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

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	Research Areas >> Others Signaling Pathways >> Others >> Others

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).

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

Symbol	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

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%

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...

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