cas 121492-06-6|| where to buy 2-(N-Boc-N-methylamino)ethylamine

製品名:2-(N-Boc-N-methylamino)ethylamine

IUPAC Name:tert-butyl N-(2-aminoethyl)-N-methylcarbamate

: CAS番号：121492-06-6; 分子式：C8H18N2O2; 純度：95%

: カタログ番号：CM117467; 分子量：174.24

包装単位	有効在庫	価格（USD）
CM117467-10g	in stock	ƴş
CM117467-25g	in stock	ǠȋǠ
CM117467-50g	in stock	œƚƴ
CM117467-100g	in stock	ƚǠǆ

問い合わせ: sales@chemenu.com

研究開発用専用.

問い合わせフォーム

化学物質名

CAS番号

数量*

要求仕様*
（アッセイ %、材料グレード等）

お名前*

連絡先Eメールアドレス*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 121492-06-6 regularly via the above email.

追記事項

Verification code*

refresh

製品詳細

: CAS番号:121492-06-6; 分子式:C8H18N2O2; 融点:-; SMILESコード:NCCN(C(OC(C)(C)C)=O)C; 密度:

: カタログ番号:CM117467; 分子量:174.24; 沸点:; MDL番号:MFCD01317789; 保管方法:

Column Infos

: Nitrogen Compounds; Nitrogen compounds can be classified as mineral or organic. Mineral compounds are essentially formed by the ammonium ion (NH4+), which is generated when ammonium salts are dissolved in water. Organic compounds, in contrast, are carbon and hydrogen compounds that contain a nitrogen atom. All organic nitrogen-containing compounds can be considered as derivatives of ammonia in which one or more hydrogen atoms are substituted by hydrocarbon radicals.

Product Other Information

Product Overview	N-Boc-N-methylethylenediamine (Boc-MEDA) is a bifunctional amine that can be used as a ligand, protecting group, and as a reagent in organic synthesis.
Synthesis Method	N-Boc-N-methylethylenediamine is synthesized through the reaction of N-Boc-N-methyl-2-aminopyridine with ethylenediamine. This reaction is typically carried out in aqueous solution at room temperature and is often catalyzed by a base, such as sodium hydroxide.
Chemical Properties	It is relatively easy to synthesize, is readily available, and is relatively inexpensive. It can be toxic if not handled properly.
Synthesis and Application	It can be used as a ligand in coordination chemistry, as a protecting group in organic synthesis, and as a reagent in organic synthesis. N-Boc-N-methylethylenediamine is also used in drug delivery, catalysis, and imaging. Additionally, N-Boc-N-methylethylenediamine is used in the synthesis of a variety of compounds, including peptides and peptidomimetics.
Future Directions	The use of N-Boc-N-methylethylenediamine as a reagent in peptide synthesis, as a stabilizer in drug delivery, and as a catalyst in catalysis. Additionally, future research could focus on the development of new methods for the synthesis of N-Boc-N-methylethylenediamine, as well as the development of new methods for the use of N-Boc-N-methylethylenediamine in laboratory experiments. Furthermore, future research could focus on the development of new methods for the detection and quantification of N-Boc-N-methylethylenediamine in biological samples. Finally, future research could focus on the development of new methods for the delivery of N-Boc-N-methylethylenediamine to specific areas of the body.