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

$284.89 - $955.10

Chemical Identifiers

CAS 334999-32-5
Molecular Formula C11H21ClN2O4
Molecular Weight (g/mol) 280.75
MDL Number MFCD03787929
InChI Key KFYCQKLSGMAVQH-WLYNEOFISA-N
Synonym 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
PubChem CID 17750455
SMILES [H+].[Cl-].COC(=O)[C@@H]1C[C@@H](N)CN1C(=O)OC(C)(C)C
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Products 2
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAH5256603
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Thermo Scientific Chemicals
H5256603
1 g
Each for $284.89
 
AAH5256606
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Thermo Scientific Chemicals
H5256606
5 g
Each for $955.10
 
Description

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.
Specifications

Chemical Identifiers

334999-32-5
280.75
KFYCQKLSGMAVQH-WLYNEOFISA-N
17750455
C11H21ClN2O4
MFCD03787929
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
[H+].[Cl-].COC(=O)[C@@H]1C[C@@H](N)CN1C(=O)OC(C)(C)C

Specifications

334999-32-5
MFCD03787929
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
[H+].[Cl-].COC(=O)[C@@H]1C[C@@H](N)CN1C(=O)OC(C)(C)C
280.75
280.75
trans-4-Amino-N-Boc-L-proline methyl ester hydrochloride
C11H21ClN2O4
1 g
KFYCQKLSGMAVQH-WLYNEOFISA-N
hydrogen 1-tert-butyl 2-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylate chloride
17750455
97%
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Safety and Handling

Safety and Handling

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only