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  6. 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%, Thermo Scientific Chemicals

Catalog Number p-7034866
Click to view available options
Quantity:
250 mg
1 g
5 g
334999-32-5
C11H21ClN2O4
280.75
MFCD03787929
KFYCQKLSGMAVQH-WLYNEOFISA-N
2s,4r-1-tert-butyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride, n-boc-trans-4-amino-l-proline methyl ester hydrochloride, 2s,4r-1-boc-4-amino-l-proline methyl ester hcl, 2s,4r-4-amino-1-boc-pyrrolidine-2-carboxylic acid methyl ester-hcl, 1-tert-butyl 2-methyl 2s,4r-4-aminopyrrolidine-1,2-dicarboxylate hydrochloride, n-boc-trans-4-amino-l-proline methyl ester hydrochloride salt, methyl trans-3-amino-1-boc-5-pyrrolidinecarboxylate hcl, boc-trans-4-amino-l-proline methyl ester hydrochloride salt, 2s,4r-1-boc-4-amino-l-proline methyl ester hydrochloride, n-boc-trans-4-amino-l-proline methyl ester, hydrochloride salt
17750455
[H+].[Cl-].COC(=O)[C@@H]1C[C@@H](N)CN1C(=O)OC(C)(C)C
334999-32-5
C11H21ClN2O4
280.75
MFCD03787929
KFYCQKLSGMAVQH-WLYNEOFISA-N
2s,4r-1-tert-butyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride, n-boc-trans-4-amino-l-proline methyl ester hydrochloride, 2s,4r-1-boc-4-amino-l-proline methyl ester hcl, 2s,4r-4-amino-1-boc-pyrrolidine-2-carboxylic acid methyl ester-hcl, 1-tert-butyl 2-methyl 2s,4r-4-aminopyrrolidine-1,2-dicarboxylate hydrochloride, n-boc-trans-4-amino-l-proline methyl ester hydrochloride salt, methyl trans-3-amino-1-boc-5-pyrrolidinecarboxylate hcl, boc-trans-4-amino-l-proline methyl ester hydrochloride salt, 2s,4r-1-boc-4-amino-l-proline methyl ester hydrochloride, n-boc-trans-4-amino-l-proline methyl ester, hydrochloride salt
17750455
[H+].[Cl-].COC(=O)[C@@H]1C[C@@H](N)CN1C(=O)OC(C)(C)C

Description

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.
TRUSTED_SUSTAINABILITY
Quantity 250 mg
IUPAC Name 1-O-tert-butyl 2-O-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylate;hydrochloride
Formula Weight 280.75
Percent Purity 97%
Chemical Name or Material trans-4-Amino-N-Boc-L-proline methyl ester hydrochloride

Safety and Handling

TSCA No
Recommended Storage Ambient temperatures
SDS

RUO – Research Use Only

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