3,4-Dimethoxyphenylacetone, 97%
3,4-Dimethoxyphenylacetone, 97%
3,4-Dimethoxyphenylacetone, 97%
Thermo Scientific Chemicals

3,4-Dimethoxyphenylacetone, 97%

CAS: 776-99-8 | C11H14O3 | 194.23 g/mol
製品番号(カタログ番号) L05477.18
または、製品番号L05477-18
価格(JPY)
-
数量:
50 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS776-99-8
Appearance (Color)Clear, yellow to yellow-green
Refractive Index1.5330-1.5380 @ 20?C
FormLiquid
Assay (GC)>96.0%
3,4-Dimethoxyphenylacetone was used as starting material in the synthesis of α-methyl-dopa, an important nonproteogenic α-amino acid for pharmaceutical applications. 3,4-Dimethoxyphenylacetone undergoes asymmetric amination catalyzed by Brevibacterium linens IFO 12141 strain to yield corresponding optically active amine

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3,4-Dimethoxyphenylacetone was used as starting material in the synthesis of α-methyl-dopa, an important nonproteogenic α-amino acid for pharmaceutical applications. 3,4-Dimethoxyphenylacetone undergoes asymmetric amination catalyzed by Brevibacterium linens IFO 12141 strain to yield corresponding optically active amine

Solubility
Insoluble in water.

Notes
Stable under normal temperatures and pressures. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents.
RUO – Research Use Only

General References:

  1. W H Boesten et. al. Asymmetric strecker synthesis of alpha-amino acids via a crystallization-induced asymmetric transformation using (R)-phenylglycine amide as chiral auxiliary. Organic letters. 2001, 3,(8), 1121-1124.
  2. Nakamichi K, et al. Asymmetric amination of 4-methoxyphenylacetone and its related compounds with microorganisms. Appl. Microbiol. Biotechnol. 1990, 33,(6), 637-640.