trans-4-Amino-N-Boc-L-proline methyl ester hydrochloride, 97%
trans-4-Amino-N-Boc-L-proline methyl ester hydrochloride, 97%
trans-4-Amino-N-Boc-L-proline methyl ester hydrochloride, 97%
Thermo Scientific Chemicals

trans-4-Amino-N-Boc-L-proline methyl ester hydrochloride, 97%

CAS: 334999-32-5 | C11H21ClN2O4 | 280.75 g/mol
製品番号(カタログ番号) H52566.06
または、製品番号H52566-06
価格(JPY)
-
数量:
5 g
一括またはカスタム形式をリクエストする
仕様
CAS334999-32-5
化学物質名または材質trans-4-Amino-N-Boc-L-proline methyl ester hydrochloride
式量280.75
IUPAC名1-O-tert-butyl 2-O-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylate;hydrochloride
InChIキーKFYCQKLSGMAVQH-WLYNEOFISA-N
さらに表示
trans-4-Amino-N-Boc-L-proline methyl ester hydrochloride acts as a pharmaceutical intermediate. It is used to prepare N-Boc-protected proline methyl ester of calix[4]arene, which is efficiently catalyzes the enantioselective aldol reaction.

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
trans-4-Amino-N-Boc-L-proline methyl ester hydrochloride acts as a pharmaceutical intermediate. It is used to prepare N-Boc-protected proline methyl ester of calix[4]arene, which is efficiently catalyzes the enantioselective aldol reaction.

Notes
Store in a cool place. Moisture sensitive. Incompatible with oxidizing agents and acids.
RUO – Research Use Only
Hahnenkamp, A.; Schäfers, M.; Bremer, C.; Höltke, C. Design and synthesis of small-molecule fluorescent photoprobes targeted to aminopeptdase N (APN/CD13) for optical imaging of angiogenesis. Bioconjugate Chem. 2013, 27 (6), 1027-1038.