CAS 2240-25-7|6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE

Introduction:Basic information about CAS 2240-25-7|6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE
CAS Number2240-25-7Molecular Weight190.00
Density1.3±0.1 g/cm3Boiling Point359.5±42.0 °C at 760 mmHg
Molecular FormulaC4H4BrN3OMelting Point240-243ºC
MSDSUSAFlash Point171.2±27.9 °C
Symbol
GHS05, GHS07
Signal WordDanger

Names

Name6-amino-5-bromo-1H-pyrimidin-2-one
SynonymMore Synonyms

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

Description4-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 CatalogResearch Areas >>OthersSignaling Pathways >>Others >>Others

Chemical & Physical Properties

Density1.3±0.1 g/cm3
Boiling Point359.5±42.0 °C at 760 mmHg
Melting Point240-243ºC
Molecular FormulaC4H4BrN3O
Molecular Weight190.00
Flash Point171.2±27.9 °C
Exact Mass263.071320
PSA72.03000
LogP3.14
Vapour Pressure0.0±0.8 mmHg at 25°C
Index of Refraction1.583
InChIKeyQFVKLKDEXOWFSL-UHFFFAOYSA-N
SMILESNc1[nH]c(=O)ncc1Br
Water SolubilitySoluble in formic acid (50 mg/ml).

Safety Information

Symbol
GHS05, GHS07
Signal WordDanger
Hazard StatementsH302-H315-H317-H318-H335
Precautionary StatementsP261-P280-P305 + P351 + P338
Hazard CodesXn
Risk Phrases22-37/38-41-43-48-20/21/22
Safety PhrasesS22-S24/25
RIDADRNONH for all modes of transport
WGK Germany3
HS Code2933599090

Customs

HS Code2933599090
Summary2933599090. 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
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