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
N-Cyclopentyl-3-(4-pyridinyl)-1,2,4-oxadiazole-5-methanamine
Tert-butyl (1-benzylcyclopropyl)carbamate
(1R)-1-(2-Fluoro-4-methoxyphenyl)ethane-1,2-diamine
(1R)-1-(4-Chloro-2-fluoro-phenyl)ethane-1,2-diamine
Methyl 5-aminoquinoline-6-carboxylate
3-(2-Cyclopropylethoxy)aniline
Tetradec-13-yn-1-amine
(1S,3S)-3-Methoxycyclopentane-1-carboxylic acid
2-Amino-4-iodobenzamide
3-(6-chloro-1H-indol-1-yl)propan-1-amine

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