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O-tert-Butyl-L-threonine, 98%|203962|4378-13-6

O-tert-Butyl-L-threonine, 98%

Cat. No JKB12168_1_G
J&K Chemical

Product Information

Product Name
O-tert-Butyl-L-threonine, 98%
Brand Name
J&K
Product Number
203962
CAS
4378-13-6
Molecular Formula
C8H17NO3
Molecular Weight
175.23
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
H-Thr(tBu)-OH
PubChem CID
6951357
IUPAC Name
(2S,3R)-2-amino-3-(2-methylpropan-2-yl)oxybutanoic acid
InChI Key
NMJINEMBBQVPGY-RITPCOANSA-N
SMILES
CC@H(C@@H(C(=O)O)N)OC(C)(C)C

Properties

Melting Point
244-247
Optical Activity
-46.0° to -42.0° (C=2, MeOH)

Safety Information

Precautionary Statement
P262

References Data Source From Pubchem

Prospects for the structure‒function evolution of SARS-CoV-2 main protease inhibitors
Publication Name: Journal of Computer-Aided Molecular Design
Publication Date: 2025-09-15
DOI: 10.1007/s10822-025-00654-9

Ligand-based and structure-based studies to develop predictive models for SARS-CoV-2 main protease inhibitors through the 3d-qsar.com portal
Publication Name: Journal of Computer-Aided Molecular Design
Publication Date: 2022-06-18
DOI: 10.1007/s10822-022-00460-7

Incorporation of Azide and Alkyne Functionalities into Peptides
Publication Name: Science of Synthesis
Publication Date: 2021

Three-Component Reaction of Ketones, Amines, and Aldehydes via Enamine Catalysis
Publication Name: Science of Synthesis
Publication Date: 2017

Development of an Amino Acid/Hydroxy Oxime Dual Catalyst System for Highly Stereoselective Direct Asymmetric Aldol Reactions in the Presence of Water
Publication Name: Synthesis
Publication Date: 2016-11-04
DOI: 10.1055/s-0036-1588089

O-tert-Butyl-L-threonine, 98%

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