Trans-4-amino-1-n-boc-3-pyrrolidinecarboxylic acid ethyl ester hcl


Chemical Name: Trans-4-amino-1-n-boc-3-pyrrolidinecarboxylic acid ethyl ester hcl
CAS Number: 955138-54-2
Product Number: AG00IJ6G(AGN-PC-0WAJ80)
Synonyms:
MDL No:
Molecular Formula: C12H23ClN2O4
Molecular Weight: 294.7750

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The (3S,4R)-1-tert-Butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate hydrochloride is a valuable compound widely utilized in chemical synthesis processes. Its asymmetric structure enables it to serve as a chiral building block in the creation of complex molecules, particularly in the pharmaceutical and agrochemical industries. By incorporating this compound into reactions, chemists can control the stereochemistry of the products, leading to the efficient production of enantiomerically pure compounds with high levels of selectivity. The hydrochloride form of (3S,4R)-1-tert-Butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate enhances its solubility in aqueous solutions, making it easier to handle in various synthetic transformations. This compound's versatility and effectiveness in catalyzing asymmetric reactions make it a valuable tool for chemists striving to synthesize intricate molecules with specific stereochemical properties.