5-fluoro-1,3-dimethyluracil

[ Density]:
1.37g/cm3

[ Boiling Point ]:
182.5ºC at 760mmHg

[ Melting Point ]:
132-134ºC(lit.)

[ Molecular Formula ]:
C₆H₇FN₂O₂

[ Molecular Weight ]:
158.13000

[ Flash Point ]:
64.1ºC

[ Exact Mass ]:
158.04900

[ PSA ]:
44.00000

[ Index of Refraction ]:
1.529

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

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933599090

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Precursor

DownStream

[ 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%

Studies on oxidative modifications of nucleic acid pyrimidine bases.

Nucleic Acids Symp. Ser. (15) , 1-4, (1984)

Oxidation of diacetylthymidine (4), triacetyluridine (5), and 5-fluoro-1,3-dimethyluracil (3) with m-chloroperbenzoic acid and cross-linkage of the bromohydrin (6) with the benzylamine and glycine eth...

Development of diversified methods for chemical modification of the 5,6-double bond of uracil derivatives depending on active methylene compounds.

Molecules 17(6) , 6519-46, (2012)

The reaction of 5-halogenouracil and uridine derivatives 1 and 7 with active methylene compounds under basic conditions produced diverse and selective C-C bond formation products by virtue of the natu...

Stereoselective synthesis of tetrahydronaphthocyclobuta[1,2-d]pyrimidinediones from 5-fluoro-1,3-dimethyluracil and naphthalenes.

Chem. Pharm. Bull. 53(2) , 258-9, (2005)

Upon UV-irradiation in the presence of piperylene, 5-fluoro-1,3-dimethyluracil (5-FDMU) couples with naphthalenes having either an electron-withdrawing group or an electron-donating group by way of 1,...

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