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N-Boc-D-proline, 99%|297390|37784-17-1

N-Boc-D-proline, 99%

Cat. No JKB10097_100_G
J&K Chemical

Product Information

Product Name
N-Boc-D-proline, 99%
Brand Name
J&K
Product Number
297390
CAS
37784-17-1
Molecular Formula
C10H17NO4
Molecular Weight
215.25
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
N-(tert-Butoxycarbonyl)-D-proline
PubChem CID
688022
IUPAC Name
(2R)-1-(2-methylpropan-2-yl)oxycarbonylpyrrolidine-2-carboxylic acid
InChI Key
ZQEBQGAAWMOMAI-SSDOTTSWSA-N
SMILES
CC(C)(C)OC(=O)N1CCCC@@H1C(=O)O

Properties

Melting Point
134-137
Optical Activity
59°to 62°(C=1, CH3COOH)

Safety Information

Precautionary Statement
P262
Storage Condition
Store at 2-8℃

References Data Source From Pubchem

Asymmetric synthesis of enantioenriched lactams from cyclic ketones via Beckmann rearrangement
Publication Name: Nature Chemistry
Publication Date: 2026-02-13
DOI: 10.1038/s41557-026-02068-y

Enantioselective Benzylic C—H Oxidation
Publication Name: Science of Synthesis
Publication Date: 2023

Applications of the Horner–Wadsworth–Emmons Olefination in Modern Natural Product Synthesis
Publication Name: Synthesis
Publication Date: 2021-06-24
DOI: 10.1055/a-1493-6331

Synthesis of novel phase transfer catalysts derived from proline-mandelic acid/tartaric acid: their evaluation in enantioselective epoxidation and Darzen condensation
Publication Name: Journal of Chemical Sciences
Publication Date: 2019-02-23
DOI: 10.1007/s12039-019-1597-6|10.1007/s12039-019-1642-5

Proline-Glycine Dipeptidic Derivatives of Chiral Phosphoramides as Organocatalysts for the Enantiodivergent Aldol Reaction of Aryl Aldehydes and Isatins with Cyclohexanone in the Presence of Water
Publication Name: Synthesis
Publication Date: 2018-05-29
DOI: 10.1055/s-0036-1592005

N-Boc-D-proline, 99%

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