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100858-33-1
1-Pyrrolidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester, (3R)-

Catalog#:1P0003HY

CAS:100858-33-1

MDL:MFCD07368258

Molecular Formula:C12H15NO3

Molecular Weight:221.2524

UN Number:

Haz Class:

Packing Group:

Synonyms: 100858-33-1; (R)-(-)-1-Cbz-3-pyrrolidinol; PubChem18734; (R)-N-Z-3-Pyrrolidinol; 1-Pyrrolidinecarboxylicacid, 3-hydroxy-, phenylmethyl ester, (3R)-; 3-Hydroxy-Cbz-(R)Pyrrolidine; SCHEMBL1841984; (3R)-3-HYDROXY-1-PYRROLIDINECARBOXYLICACID PHENYLMETHYL ESTER; 3-Hydroxy-Cbz-(R)-pyrrolidine; CTK3J9308; (R)-3-Hydroxy-pyrrolidine-1-carboxylic acid benzyl ester; DTXSID20457976; benzyl (3R)-3-hydroxypyrrolidine-1-carboxylate; MBLJFGOKYTZKMH-LLVKDONJSA-N; (3R)-N-CBZ-3-PYRROLIDINOL; 0281AA; ANW-43207; CC0033; MFCD07368258; ZINC16697505; AKOS016842292; ACN-052013; CC-1669; (R)-Benzyl 3-hydroxypyrrolidine-1-carboxylate; CS-W003377; DS-0808; FS-2448; PB13059; (R)-1-Benzyloxycarbonyl-3-pyrrolidinol; KS-0000032I; (R)-1-Carbobenzoxy-3-hydroxypyrrolidine; AC-22438; AJ-69355; BR-32647; (R)-1-CBZ-3-PYRROLIDINOL; CJ-15599; (R)-(-)-1-Cbz-3-pyrrolidinol, 95%; (R)-(−)-1-Cbz-3-pyrrolidinol; AB0063004; DB-024529; RT-004952; ST2408107; (R)-N-benzyloxycarbonyl-3-hydroxypyrrolidine; FT-0648067; n-benzyloxycarbonyl-(r)-3-hydroxypyrrolidine; (R)-N-Cbz-3-hydroxypyrrolidine; TL80090966; (3R)-N-benzyloxycarbonyl-3-hydroxypyrrolidine; benzyl (R)-3-hydroxypyrrolidine-1-carboxylate; (3R)-N- benzyloxycarbonyl-3-hydroxypyrrolidine; benzyl (R)-3-hydroxy-pyrrolidine-1-carboxylate; Benzyl(3R)-3-hydroxypyrrolidine-1-carboxylate; S-1808; Benzyl (3R)-3-hydroxy-1-pyrrolidinecarboxylate; 858C331; J-000239; (R)-1-Carbobenzoxy-3-pyrrolidinol; (R)-(-)-1-Benzyloxycarbonyl-3-hydroxypyrrolidine, 95%; 3alpha-Hydroxypyrrolidine-1-carboxylic acid benzyl ester; (R)-3-hydroxy-1-pyrrolidinecarboxylic acid, phenylmethyl ester; C13H17NO3; ?(-)-N-Cbz-3-hydroxypyrrolidine; ACN-S002112; CB12008; CID11183628; Benzyl 3-hydroxy-1-pyrrolidinecarboxylate; C2585; (R)-1-CBZL-3-PYRROLIDINOL; (R)-Benzyl 3-hydroxypiperidine-1-carboxylate; (R)-1-Cbz-3-pyrrolidinol, 98%, ee: 98% - 1G 1g; 100858-34-2; (R)-(-)-1-Cbz-3-Hydroxy-pyrrolidine; 1-PYRROLIDINECARBOXYLIC ACID, 3-HYDROXY-, PHENYLMETHYL ESTER, (3R)-;

Keywords: 100858-33-1,MFCD07368258,1P0003HY,1-Pyrrolidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester, (3R)-,C12H15NO3

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P0003HY 98% 1g $10.00 $8.00 In Stock USA ADD TO CART BUY NOW
1P0003HY 98% 5g $20.00 $15.00 In Stock USA ADD TO CART BUY NOW
1P0003HY 95% 10g $24.00 $18.00 In Stock USA ADD TO CART BUY NOW
1P0003HY 95% 25g $50.00 $37.00 In Stock USA ADD TO CART BUY NOW
1P0003HY 95% 50g $96.00 $72.00 In Stock USA ADD TO CART BUY NOW 

  • 1-Pyrrolidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester, (3R)- is a compound with specific stereochemistry and functional groups that make it useful in chemical synthesis. Let's explore some of its key applications:

1. **Asymmetric Synthesis**: The (3R)-configuration of 1-pyrrolidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester imparts chirality to the molecule. This compound can serve as a chiral building block in asymmetric synthesis, enabling the stereoselective formation of other compounds. Asymmetric synthesis is essential in pharmaceutical chemistry for the production of enantiomerically pure drugs, as well as in the synthesis of chiral ligands and catalysts.

2. **Medicinal Chemistry**: Compounds derived from 1-pyrrolidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester may exhibit pharmacological activities and are investigated for their potential therapeutic applications. The presence of the phenylmethyl ester and hydroxy groups can influence the compound's interactions with biological targets, making it a valuable scaffold for drug design. This compound and its derivatives can serve as precursors or intermediates in the synthesis of pharmaceutical agents targeting various diseases.

3. **Peptide Synthesis**: The carboxylic acid group in 1-pyrrolidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester can serve as a protecting group for amino acids in peptide synthesis. Peptides are important biomolecules with diverse biological activities, and the ability to synthesize them efficiently is crucial for drug discovery and biomedical research. By using this compound as a protecting group, specific functional groups on amino acids can be selectively protected, allowing for controlled peptide synthesis.

4. **Organic Synthesis**: 1-Pyrrolidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester can undergo various chemical transformations, including esterification, amidation, and substitution reactions. These reactions enable the synthesis of a wide range of organic compounds, including heterocyclic compounds, amino acids, and pharmaceutical intermediates. The presence of the phenylmethyl ester moiety provides opportunities for further functionalization and diversification of the molecule.

5. **Catalysis**: Certain derivatives of 1-pyrrolidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester may exhibit catalytic activity in organic reactions. They can serve as catalysts or co-catalysts in various transformations, including hydrogenation, oxidation, and cross-coupling reactions. Catalytic applications of this compound can enable more efficient and selective synthesis of organic molecules.

Overall, 1-Pyrrolidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester, (3R)- offers diverse applications in asymmetric synthesis, medicinal chemistry, peptide synthesis, organic synthesis, and catalysis, making it a valuable compound in chemical synthesis and related fields.

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