CAS 2775-87-3

Fórmula: C11H8N2O3

InChI: InChI=1S/C11H8N2O3/c14-9-6-7-12-11(16)13(9)10(15)8-4-2-1-3-5-8/h1-7H,(H,12,16)

Chave InChI: RJAJHSYADHZMNA-UHFFFAOYSA-N

SMILES: C1=CC=C(C=C1)C(=O)N2C(=O)C=CNC2=O

3-Benzoylpyrimidine-2,4(1H,3H)-dione

CAS: 2775-87-3

3-Benzoylpyrimidine-2,4(1H,3H)-dione

Fórmula: C₁₁H₈N₂O₃

Pureza: 98%

Peso molecular: 216.2

Ref: 54-OR1001380

3-Benzoylpyrimidine-2,4(1H,3H)-dione

CAS: 2775-87-3

Fórmula: C₁₁H₈N₂O₃

Pureza: 98%

Cor e Forma: Solid

Peso molecular: 216.1928

Ref: IN-DA002UNN

3-Benzoylpyrimidine-2,4(1H,3H)-dione

CAS: 2775-87-3

Pureza: 98%

Peso molecular: 216.1959991

Ref: 10-F604605

3-Benzoyl-1H-pyrimidine-2,4-dione

CAS: 2775-87-3

3-Benzoyl-1H-pyrimidine-2,4-dione is a nucleobase analogue that can be used as an acceptor in phosphonate hybridization assays. It has been shown to be a substrate for the benzyl group and undergoes arylations with various electrophiles such as thiophenol and acetyl chloride. 3-Benzoyl-1H-pyrimidine-2,4-dione can also undergo conjugations with various carboxylic acids such as benzoic acid or 4-(dimethylamino)benzoic acid. This compound has been synthesized by reacting cyclobutanone with 3,5-dibromopyridine in the presence of potassium carbonate and sodium bicarbonate to produce 3-(benzoyl)-1H-pyrimidine-2,4(3H)-dione. This reaction was followed by hydrolysis of the

Fórmula: C₁₁H₈N₂O₃

Pureza: Min. 95%

Peso molecular: 216.19 g/mol

Ref: 3D-CAA77587