5-Iodo-2,4-dimethoxypyrimidine

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Names

[ Name ]:
5-Iodo-2,4-dimethoxypyrimidine

[Synonym ]:
5-Iodo-2,4-dimethoxypyrimidine
Pyrimidine, 5-iodo-2,4-dimethoxy-
MFCD00090865
5-iodo-2,6-dimethoxypyrimidine
5-iododimethoxypyrimidine
2,4-Dimethoxy-5-iodo-pyrimidine
2,4-dimethoxy pyrimidin-5-yl iodide
5-iodo-2,4-dimethoxy-pyrimidine

Chemical & Physical Properties

[ Density]:
1.8±0.1 g/cm3

[ Boiling Point ]:
328.7±52.0 °C at 760 mmHg

[ Melting Point ]:
71-75 °C(lit.)

[ Molecular Formula ]:
C₆H₇IN₂O₂

[ Molecular Weight ]:
266.036

[ Flash Point ]:
152.6±30.7 °C

[ Exact Mass ]:
265.955200

[ PSA ]:
44.24000

[ LogP ]:
2.44

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.582

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

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

[ Hazard Codes ]:
Xi,T

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933599090

Synthetic Route

Click to get detail synthetic route

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)

Nucleic acid components and their analogues. XLIII. Synthesis of anomeric 5-iodo-2'-deoxyuridines. Prystaš M and Šorm F.

Collect. Czech. Chem. Commun. 29(1) , 121-30, (1964)

Synthesis of nucleosides. 9. General synthesis of N-glycosides. I. Synthesis of pyrimidine nucleosides. Niedballa U and Vorbrüggen H.

J. Org. Chem. 39(25) , 3654-3660, (1974)

5-iodo-2,4,7-trinitro-fluoren-9-one; triphenylene
5-Iodo-2-[(4-methyl-3-nitrobenzoyl)amino]benzoic acid
5-IODO-2-[[[(4-PROPOXYBENZOYL)AMINO]THIOXOMETHYL]AMINO]-BENZOIC ACID
5-iodo-2,4-bis-O-trimethylsilyluracil
5-iodo-2-((4-iodophenyl)diazenyl)phenol
5-iodo-2-[[[[4-(phenoxymethyl)benzoyl]amino]thioxomethyl]amino]-benzoic acid
1-Methylcyclopentyl 4-methylbenzene-1-sulfonate
2-Bromo-5-(fluoromethoxy)pyridine
2-(5-Fluoro-2-methylphenyl)prop-2-enoic acid
7-[(2S,3R,4S,5S,6R)-4,5-Dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one
1-[(5S,8R,10S,13S)-3-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-16-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone
(4As,6aS,6bR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4-hydroxy-3,5-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
(2S,3S,4S,5R,6R)-6-[[(3S,4S,6aR,6bS,8aS,12aS,14bR)-4-formyl-8a-[(2S,3R,4S,5R,6R)-4-hydroxy-3-[(2S,3R,4S,5S,6S)-3-hydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]oxy-6-methyloxan-2-yl]oxycarbonyl-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-hydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3
1-[2-[(4-Methoxyphenyl)methyl]pyrazol-3-yl]ethanone
4-Chloro-5-ethynylthiazole
2-(tert-Butyl)-5-ethynylthiazole

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