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N-Boc-L-serine β-lactone, 98%|439836|98541-64-1

N-Boc-L-serine β-lactone, 98%

Cat. No JK439836_1_G
J&K Chemical

Product Information

Product Name
N-Boc-L-serine β-lactone, 98%
Brand Name
J&K
Product Number
439836
CAS
98541-64-1
Molecular Formula
C8H13NO4
Molecular Weight
187.20
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
(S)-N-(tert-Butoxycarbonyl)-3-amino-2-oxetanone
PubChem CID
2763194
IUPAC Name
tert-butyl N-(3S)-2-oxooxetan-3-ylcarbamate
InChI Key
HRJDEHQWXAPGBG-YFKPBYRVSA-N
SMILES
CC(C)(C)OC(=O)NC@H1COC1=O

Properties

Optical Activity
-31 to -21 (C=1, CH3CN)

Safety Information

Precautionary Statement
P262
Storage Condition
Store at 2-8℃

References Data Source From Pubchem

Advances in the Synthesis of Enterobactin, Artificial Analogues, and Enterobactin-Derived Antimicrobial Drug Conjugates and Imaging Tools for Infection Diagnosis
Publication Name: Synthesis
Publication Date: 2022-05-17
DOI: 10.1055/a-1783-0751

Synthesis of Azido Acids and Their Application in the Preparation of Complex Peptides
Publication Name: Synthesis
Publication Date: 2020-11-09
DOI: 10.1055/s-0040-1707314

N-(2-Oxo-3-oxetanyl)carbamic Acid Esters as N-Acylethanolamine Acid Amidase Inhibitors: Synthesis and Structure–Activity and Structure–Property Relationships
Publication Name: Journal of Medicinal Chemistry
Publication Date: 2012-05-10
DOI: 10.1021/jm300349j

Michael-type Addition as a Convenient Method for Regioselective N-Alkylation of Ambident Uracils
Publication Name: Synthesis
Publication Date: 2010-04-28
DOI: 10.1055/s-0029-1218757

By Reaction with Lactones
Publication Name: Science of Synthesis
Publication Date: 2008

N-Boc-L-serine β-lactone, 98%

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