CAS 208264-53-3

Fórmula: C5H4BrNOS

InChI: InChI=1S/C5H4BrNOS/c1-3(8)5-7-4(6)2-9-5/h2H,1H3

Chave InChI: YQJROTDRGHSQNZ-UHFFFAOYSA-N

SMILES: CC(=O)C1=NC(=CS1)Br

1-(4-Bromothiazol-2-yl)ethan-1-one

CAS: 208264-53-3

1-(4-Bromothiazol-2-yl)ethan-1-one

Fórmula: C₅H₄BrNOS

Pureza: 97%

Peso molecular: 206.06

Ref: 54-OR77489

1-(4-Bromothiazol-2-yl)ethanone

CAS: 208264-53-3

Fórmula: C₅H₄BrNOS

Pureza: 97%

Cor e Forma: Solid

Peso molecular: 206.0604

Ref: IN-DA002JM8

1-(4-Bromothiazol-2-yl)ethanone

CAS: 208264-53-3

1-(4-Bromothiazol-2-yl)ethanone

Fórmula: C₅H₄BrNOS

Pureza: 97%

Peso molecular: 206.06

Ref: IN-DG627551

1-(4-Bromothiazol-2-yl)ethanone

CAS: 208264-53-3

Fórmula: C₅H₄BrNOS

Pureza: 97%

Cor e Forma: Solid

Peso molecular: 206.06

Ref: 10-F545108

2-Acetyl-4-bromothiazole

CAS: 208264-53-3

2-Acetyl-4-bromothiazole (ABT) is a bromoketone that has been used as an efficient and multigram active compound in the synthesis of trimethyltin. ABT is also used as an analogue to synthesize enantiopure thioamides with high yield and biological activity. This compound can be used for the asymmetric synthesis of enantiomers. It was first prepared by reacting 4-bromoacetophenone with sodium methoxide in methanol, followed by acetylation of the resulting 2-acetylthiazole with acetic anhydride.

Fórmula: C₅H₄BrNOS

Pureza: Min. 95%

Peso molecular: 206.06 g/mol

Ref: 3D-IIA26453