2,4-Dimethoxy-5-bromopyrimidine

Names

[ Name ]:
2,4-Dimethoxy-5-bromopyrimidine

[Synonym ]:
2,4-Dimethoxy-5-bromopyrimidine
Pyrimidine, 5-bromo-2,4-dimethoxy-
MFCD00038016
5-Bromo-2,4-dimethoxypyrimidine

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
297.0±43.0 °C at 760 mmHg

[ Melting Point ]:
62-65 °C(lit.)

[ Molecular Formula ]:
C₆H₇BrN₂O₂

[ Molecular Weight ]:
219.036

[ Flash Point ]:
133.4±28.2 °C

[ Exact Mass ]:
217.969086

[ PSA ]:
44.24000

[ LogP ]:
1.87

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.533

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi,Xn

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933599090

Precursor & DownStream

Precursor

2,4-Dimethoxypyrimidine
Methanol
5-Bromo-2,4-dichloropyrimidine
Sodium Methylate

DownStream

2,4-Dimethoxypyrimidine
2-(2,4-dimethoxypyrimidin-5-yl)-7,14-dioxa-1-azadispiro[4.2.5.2]pentadec-1-ene 1-oxide
5-(2,2-dichloro-1-fluorovinyl)-2,4-dimethoxypyrimidine
2,4-dimethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine
5-Ethyluracil
2,4-Dimethoxy-5-methylpyrimidine
5-Bromouracil
Thymine
5-formyl-2,4-dimethoxypyrimidine

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%

Articles

Palladium-catalysed carbomethoxyvinylation and thienylation of 5-iodo (bromo)-2, 4-dimethoxypyrimidine in water. Basnak I, et al.

Tetrahedron Lett. 38(27) , 4869-72, (1997)

The Hilbert-Johnson Reaction of 2, 4-Dialkoxypyrimidines with Halogenoses. Pliml J and Prystaš M.

Adv. Heterocycl. Chem. 8 , 115-42, (1967)

1016. Reactions of pyrimidin-5-yl-lithium compounds. Caton MPL, et al.

J. Chem. Soc. , 5467-5473, (1965)

2,4-dimethoxy-5,5,6-trimethyl-1,3,2-dioxaborinane
(2,4-dimethoxy-5-methylphenyl)-(2,5-dimethoxyphenyl)methanone
2,4-Dimethoxy-5-methylpyrimidine
2,4-dimethoxy-5-(methylthio)benzene-1-sulfonyl chloride
2,4-Dimethoxy-5-nitrobenzoic acid
2,4-dimethoxy-5,6-dimethylpyrimidine
N~1~-cyclopentyl-4-oxo-4-[4-(2-pyridyl)piperazino]butanamide
3,4,5-trimethoxy-N-[2-(methoxymethyl)-1H-benzimidazol-5-yl]benzamide
N-(3-chlorobenzyl)-2-[3-(4-fluoro-2-methoxyphenyl)-6-oxopyridazin-1(6H)-yl]acetamide
3,4,5-trimethoxy-N-(2-methyl-1H-benzimidazol-5-yl)benzamide
N-[2-(2-methoxyphenyl)ethyl]-2-[6-oxo-3-(4-phenylpiperazin-1-yl)pyridazin-1(6H)-yl]acetamide
propan-2-yl [3-(3-methoxyphenyl)-6-oxopyridazin-1(6H)-yl]acetate
N-(4-tert-butylphenyl)-2-([1,2,4]triazolo[4,3-b]pyridazin-6-ylsulfanyl)acetamide
4-benzyl-N-(2-{[(2Z)-5-methyl-1,3,4-thiadiazol-2(3H)-ylidene]amino}-2-oxoethyl)piperazine-1-carboxamide
N-[3-(acetylamino)phenyl]-2-([1,2,4]triazolo[4,3-b]pyridazin-6-ylsulfanyl)acetamide
N-(2-chlorobenzyl)-2-[3-(4-fluoro-2-methoxyphenyl)-6-oxopyridazin-1(6H)-yl]acetamide

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