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5-FLUORO-1,3-DIMETHYLURACIL

5-FLUORO-1,3-DIMETHYLURACIL Structure
CAS No.
3013-92-1
Chemical Name:
5-FLUORO-1,3-DIMETHYLURACIL
Synonyms
Fluorouracil-001;Fluorouracil Impurity 34;1,3-dimethyl-5-fluorouracil;5-FLUORO-1,3-DIMETHYLURACIL;5-Fluoro-1,3-dimethyluracil 99%;5-fluoro-1,3-dimethylpyrimidine-2,4-dione;5-fluoro-1,3-diMethylpyriMidine-2,4(1H,3H)-dione;2,4(1H,3H)-Pyrimidinedione,5-fluoro-1,3-dimethyl-;1,3-Dimethyl-5-fluorouracil, 2,4-Dihydroxy-1,3-dimethyl-5-fluoropyrimidine
CBNumber:
CB8116404
Molecular Formula:
C6H7FN2O2
Molecular Weight:
158.13
MOL File:
3013-92-1.mol
Modify Date:
2023/7/9 8:28:05

5-FLUORO-1,3-DIMETHYLURACIL Properties

Melting point 132-134 °C(lit.)
Boiling point 182.5±50.0 °C(Predicted)
Density 1.37±0.1 g/cm3(Predicted)
pka -4.07±0.40(Predicted)
BRN 880396

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3

5-FLUORO-1,3-DIMETHYLURACIL price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 406864 5-Fluoro-1,3-dimethyluracil 99% 3013-92-1 10G ₹11225.53 2022-06-14 Buy
Product number Packaging Price Buy
406864 10G ₹11225.53 Buy

5-FLUORO-1,3-DIMETHYLURACIL Chemical Properties,Uses,Production

Uses

5-Fluoro-1,3-dimethyluracil may be used as starting material in the following processes:

  • Regioselective synthesis of tetrahydronaphthocyclobuta[1,2-d]pyrimidinediones.
  • To synthesize 5-bis(ethoxycarbonyl)methyl-1,3-dimethyluracil.
  • To synthesize new highly conjugated propenylidene derivatives via aromatic Paterno-Buchi type cycloaddition with 1-methoxynaphthalene.

Synthesis Reference(s)

Tetrahedron, 46, p. 3093, 1990 DOI: 10.1016/S0040-4020(01)88400-3

General Description

Oxidation of 5-fluoro-1,3-dimethyluracil (5-FDMU) with m-chloroperbenzoic acid has been described. It is reported as antineoplastic drug. On photoirradiation, 5-fluoro-1,3-dimethyluracil yields the trans-anti cyclobutane dimer and the cis-syn cyclobutane dimer. UV irradiation of 5-FDMU and naphthalene in a protic medium affords 5-(1-naphthyl)uracil, while in aprotic media it undergoes stereoselective 1,4-cycloaddition reaction to give a barrelene derivative. The thermochemical parameters of 5-FDMU has been determined. It reacts with substituted benzenes in the presence of trifluoroacetic acid to generate 5-aryl-1,3-dimethyluracils via photosubstitution.

5-FLUORO-1,3-DIMETHYLURACIL Preparation Products And Raw materials

Raw materials

Preparation Products

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1,3-Dimethyl-5-fluorouracil, 2,4-Dihydroxy-1,3-dimethyl-5-fluoropyrimidine 5-fluoro-1,3-diMethylpyriMidine-2,4(1H,3H)-dione 5-FLUORO-1,3-DIMETHYLURACIL 1,3-dimethyl-5-fluorouracil 2,4(1H,3H)-Pyrimidinedione,5-fluoro-1,3-dimethyl- Fluorouracil-001 5-Fluoro-1,3-dimethyluracil 99% 5-fluoro-1,3-dimethylpyrimidine-2,4-dione Fluorouracil Impurity 34 3013-92-1 Building Blocks Heterocyclic Building Blocks Pyrimidines