1-Bromoadamantane - 99%min

CAS: 768-90-1

Ref. 3D-FB63507

Produktinformation

• Name: 1-Bromoadamantane - 99%min
• Synonyme: 1-Adamantyl bromide, 1-Bromo adamantine, 1-Bromoadamamtane, 1-Bromotriciclo[3.3.1.13,7]Decano, 1-Bromotricyclo(3.3.1.13,7)Decane, 1-Bromotricyclo[3.3.1.1(3,7)]decane, 1-Bromotricyclo[3.3.1.1(3.7)]decane, 1-Bromotricyclo[3.3.1.1^3,7]decane, 1-Bromotricycol[3.3.1.1.(1,7)decane, 1-Bromtricyclo[3.3.1.13,7]decan, Adamantane, 1-bromo-, Adamantyl bromide, Labotest-Bb Lt00239617, Nsc 527914, Rarechem Aq Tc 1019, Tricyclo[3.3.1.13,7]decane, 1-bromo-, Tricyclo[3.3.1.1^3,7]decane, 1-bromo-

Beschreibung

1-Bromoadamantane is a quinoline derivative that is used as a pharmaceutical preparation. It was first synthesized in the 1950s, and has been used to treat inflammatory bowel disease. The synthesis of 1-Bromoadamantane is accomplished by the palladium-catalyzed coupling of trifluoromethanesulfonic acid with an organic solution containing the bromide salt of the quinoline. The chemical structure of 1-Bromoadamantane can be seen below:

The synthesis begins with the reaction of a halide with an organosilicon compound in which one or more hydrogen atoms have been replaced by fluorine atoms, forming a fluoroalkyl halide. This reaction takes place at elevated temperatures in a solvent such as tetrahydrofuran (THF). The resulting alkene undergoes hydrolysis to form the corresponding alcohol, which is then oxidized to give either an alkyl

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 215.13 g/mol
• Formel: C₁₀H₁₅Br
• Reinheit: Min. 98.5%
• Farbe/Form: Powder
• InChl: InChI=1S/C10H15Br/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2
• InChI Key: InChIKey=VQHPRVYDKRESCL-UHFFFAOYSA-N
• SMILES: BrC12CC3CC(CC(C3)C1)C2