98854-09-2

Basic information

• Product Name: 5-BROMO-1,3-DIMETHYL-6-PHENYLURACIL
• Synonyms: 5-BROMO-1,3-DIMETHYL-6-PHENYLURACIL
• CAS NO: 98854-09-2
• Molecular Formula: C₁₂H₁₁BrN₂O₂
• Molecular Weight: 295.13
• Mol File: 98854-09-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 363.5°C at 760 mmHg
• Flash Point: 173.7°C
• Appearance: /
• Density: 1.558g/cm³
• Vapor Pressure: 1.79E-05mmHg at 25°C
• Refractive Index: 1.626
• CAS DataBase Reference: 5-BROMO-1,3-DIMETHYL-6-PHENYLURACIL(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-1,3-DIMETHYL-6-PHENYLURACIL(98854-09-2)
• EPA Substance Registry System: 5-BROMO-1,3-DIMETHYL-6-PHENYLURACIL(98854-09-2)

Safety Data

• Hazardous Substances Data: 98854-09-2(Hazardous Substances Data)

Usage

General Description

5-Bromo-1,3-dimethyl-6-phenyluracil is a synthetic chemical compound belonging to the uracil family of organic molecules. It is a derivative of uracil that contains a bromine atom at the 5th position and two methyl groups at the 1st and 3rd positions of the molecule, as well as a phenyl group attached to the 6th position. 5-BROMO-1,3-DIMETHYL-6-PHENYLURACIL is commonly used in organic synthesis and pharmaceutical research as a building block for the development of new drugs and materials. Its chemical properties make it a versatile and valuable compound for creating novel molecular structures with potential applications in various fields, such as medicine and materials science.

InChI:InChI=1/C12H11BrN2O2/c1-14-10(8-6-4-3-5-7-8)9(13)11(16)15(2)12(14)17/h3-7H,1-2H3

Upstream product

• 77-78-1 dimethyl sulfate 
• 16290-56-5 5-bromo-6-phenylpyrimidine-2,4(1H,3H)-dione 
• 7033-39-8 5-bromo-1,3-dimethyluracil 
• 591-50-4 iodobenzene 
• 79462-73-0 5,6-Dibromo-1,3-dimethyluracil 
• 71-43-2 benzene 

Relevant articles and documents

Regioselective arylation of uracil and 4-pyridone derivatives via copper(I) bromide mediated C-H bond activation

A facile and effective synthesis of 6-aryluracil derivatives was accomplished by the direct C-H bond activation for arylation. A series of 6-aryl-1,3-dimethyluracils were synthesized from the reaction of 1,3-dimethyluracil with various phenyl iodides in DMF, in the presence of copper(I) bromide as the catalyst and lithium tert-butoxide as the base. This methodology is applicable to a variety of 5-substituted uracils as well as 4-pyridone to provide direct accesses to versatile uracil and 4-pyridone derivatives.

PHOTOCHEMISTRY OF 6-HALO- AND 5,6-DIHALOURACILS. A SIMPLE SYNTHESIS OF FLUORESCENT URACIL DERIVATIVES

6-Iodo- and 5,6-dihalouracil derivatives undergo remarkably efficient photocoupling reactions leading to strongly fluorescent heterocycles in the presence of suitable radical acceptors.