5-Bromo-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione

CAS: 15018-59-4

Ref. 3D-FB128300

Product Information

• Name: 5-Bromo-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione
• Synonyms: 2,4(1H,3H)-pyrimidinedione, 5-bromo-1,3,6-trimethyl-, 2,4(1H,3H)-Pyrimidinedione, 5-bromo-1,3,6-trimethyl-, 5-Bromo-1,3,6-Trimethyluracil, 5-Bromo-1,3,6-trimethyl-2,4(1H,3H)-pyrimidinedione, 5-bromo-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione, Chembrdg-Bb 4013655, Uracil, 5-bromo-1,3,6-trimethyl-

Description

5-Bromo-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione (BTMP) is a heterocyclic compound that is used as a starting material in the synthesis of 6-methyluracil. It can be synthesized by the reaction of methyl proton with diazine to form the corresponding heterocycle. The reaction requires catalytic amounts of thiolate and a long reaction time. It is an example of nucleophilic substitution reactions that are facilitated by carbocations. The nucleophile attacks the electrophilic carbon atom, displacing the bromine atom and forming a new cationic intermediate. This cation then reacts with water to form an alcohol and a positively charged ion. In this case, the positively charged ion is protonated and transferred to another molecule or back to BTMP.

• Brand: Biosynth

Chemical properties

• Molecular weight: 233.06 g/mol
• Formula: C₇H₉BrN₂O₂
• Purity: Min. 95%
• InChI: InChI=1S/C7H9BrN2O2/c1-4-5(8)6(11)10(3)7(12)9(4)2/h1-3H3
• InChI key: InChIKey=RJNYZLOAGXCCHJ-UHFFFAOYSA-N
• SMILES: Cc1c(Br)c(=O)n(C)c(=O)n1C