CAS 728-87-0

4-Metossi-α-(4-metossifenil)benzenemetanolo

Descrizione:

4-Metossi-α-(4-metossifenil)benzenemetanolo, noto anche con il suo numero CAS 728-87-0, è un composto organico caratterizzato dalla sua complessa struttura aromatica. Presenta due gruppi metossilici (-OCH3) attaccati a un anello fenilico, il che ne migliora la solubilità nei solventi organici e contribuisce alla sua reattività chimica. La presenza del gruppo idrossile (-OH) nella porzione di benzenometanolo indica che può partecipare a legami idrogeno, influenzando le sue proprietà fisiche come i punti di ebollizione e fusione. Questo composto è tipicamente un solido bianco a bianco sporco a temperatura ambiente ed è solubile in solventi organici come etanolo e acetone. La sua struttura molecolare suggerisce potenziali applicazioni in campo farmaceutico, in particolare come precursore o intermedio nella sintesi di molecole più complesse. Inoltre, i gruppi metossilici possono conferire certe attività biologiche, rendendolo di interesse nella chimica medicinale. Tuttavia, sarebbero necessari studi dettagliati sulle sue specifiche proprietà biologiche e applicazioni per comprendere appieno i suoi potenziali utilizzi.

Formula: C₁₅H₁₆O₃

InChI: InChI=1S/C15H16O3/c1-17-13-7-3-11(4-8-13)15(16)12-5-9-14(18-2)10-6-12/h3-10,15-16H,1-2H3

InChI key: InChIKey=ZODAOVNETBTTJX-UHFFFAOYSA-N

SMILES: C(O)(C1=CC=C(OC)C=C1)C2=CC=C(OC)C=C2

Sinonimi:

• 4,4-Dimethoxydiphenylmethanol
• 4,4′-Dimethoxydiphenylcarbinol
• 4-Methoxy-4′-methoxybenzhydrol
• 4-Methoxy-Α-(4-Methoxyphenyl)Benzenemethanol
• Benzenemethanol, 4-methoxy-α-(4-methoxyphenyl)-
• Benzhydrol, 4,4′-dimethoxy-
• Bis(4-Methoxyphenyl)Methanol
• Bis(4-methoxyphenyl) carbinol
• Bis(p-methoxyphenyl)carbinol
• Bis(p-methoxyphenyl)methanol
• NSC 5256
• p,p′-Dimethoxybenzhydrol

4,4'-Dimethoxybenzhydrol

CAS: 728-87-0

Formula: C₁₅H₁₆O₃

Purezza: >98.0%(GC)

Colore e forma: White to Almost white powder to crystal

Peso molecolare: 244.29

Ref: 3B-D2141

4,4'-Dimethoxybenzhydrol, 98+%

CAS: 728-87-0

4,4?-Dimethoxybenzhydrol was used to study the kinetics and mechanism of oxidation of substituted benzhydrols to corresponding benzophenones in the presence of Hg(OAc)2 by N-bromosuccinimide. It is useful in the protection of glutamine and asparagine residues in peptide synthesis, reagent for the N-

Formula: C₁₅H₁₆O₃

Purezza: 98+%

Colore e forma: White, Powder

Peso molecolare: 244.29

Ref: 02-A14604

4,4'-DIMETHOXYBENZHYDROL

CAS: 728-87-0

Formula: C₁₅H₁₆O₃

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 244.2857

Ref: IN-DA003KDS

4,4''-Dimethoxybenzhydrol

CAS: 728-87-0

Formula: C₁₅H₁₆O₃

Peso molecolare: 244.29

Ref: 7W-GK6159

Bis(4-Methoxyphenyl)Methanol

CAS: 728-87-0

Bis(4-Methoxyphenyl)Methanol

Purezza: 98%

Peso molecolare: 244.29g/mol

Ref: 54-OR1012442

4,4'-Dimethoxybenzhydrol

CAS: 728-87-0

4,4'-Dimethoxybenzhydrol is a reaction system that has been used to control experiments in which the nucleophile is an iron catalyst. The reaction system was also used to determine the reactivity of various functional groups. The linear plot of the rate of reaction versus concentration of cyclopentenes, hydroxyl group, and dehydrated functionalities indicated that these factors had little effect on the rate of reaction. However, it was found that lactams and trifluorides were able to increase the rate of reaction. Anilines were also found to be effective as they reacted with hydrogen peroxide to form phenoxides.

Formula: C₁₅H₁₆O₃

Purezza: Min. 95%

Colore e forma: White Powder

Peso molecolare: 244.29 g/mol

Ref: 3D-FD34570

4,4′-Dimethoxybenzhydrol

CAS: 728-87-0

Formula: C₁₅H₁₆O₃

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 244.29

Ref: 10-F046791

4,4'-Dimethoxybenzhydrol

Prodotto controllato

CAS: 728-87-0

Applications 4,4'-Dimethoxybenzhydrol acts as a reagent in the preparation of aryloxyacetamide derivatives and their biological activity as neuroprotective agents. Preparation and anticancer activity of quebecol and analogs.
References Zhong, Y., et al.: Bioorg. Med. Chem. Lett., 26, 2526 (2016); Pericherla, K., et al.: Bioorg. Med. Chem. Lett., 23, 5329 (2013)

Formula: C₁₅H₁₆O₃

Colore e forma: Neat

Peso molecolare: 244.29

Ref: TR-D440130