4-Anisylchlorodiphenylmethane

CAS: 14470-28-1

Ref. 3D-FA10230

Produktinformation

• Name: 4-Anisylchlorodiphenylmethane
• Synonyme: (Chloro(-methoxyphenyl)methylene)dibenzeneMMT-Cl4-Methoxytrityl chloride4-Methoxytriphenylchloromethane4-Methoxytriphenylmethyl chloride, (p-Anisyl)diphenylmethyl chloride, 1-(Chlorodiphenylmethyl)-4-Methoxybenzene, 4-Anisyl(chloro)diphenylmethane, 4-Methoxytriphenylchloromethane, 4-Methoxytrityl chloride, 4-Monomethoxytrityl chloride, Anisole, p-(chlorodiphenylmethyl)-, Benzene, 1-(chlorodiphenylmethyl)-4-methoxy-, MMTCl, Mmt-Cl, Mono-p-methoxytrityl chloride, NSC 54121, [(Chloro)(4-methoxyphenyl)methylene]dibenzene, p-(Chlorodiphenylmethyl)anisole, p-Anisylchlorodiphenylmethane, p-Methoxytrityl chloride
• CAS: 14470-28-1

Beschreibung

4-Anisylchlorodiphenylmethane is a trifluoroacetic acid derivative of diphenyl sulfoxide. It is activated by hydrochloric acid and hydrogen chloride to form the corresponding anisyl chlorodiphenylmethane chloride. This compound has a high resistance to nucleophilic attack, with a reaction solution that is resistant to nucleophiles such as water, amines, alcohols, and carboxylic acids. 4-Anisylchlorodiphenylmethane can be synthesized from uridine and acetic acid in the presence of diphenyl sulfoxide and a base. The reaction is then heated at reflux for 24 hours. 4-Anisylchlorodiphenylmethane binds to DNA as well as RNA templates in vitro and can be used for linear regression analysis of DNA sequences. It also has inhibitory effects on cell growth in culture.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 308.8 g/mol
• Formel: C₂₀H₁₇ClO
• Reinheit: Min. 95%
• Farbe/Form: White Powder