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

Name: O-tert-Butyl-L-threonine, 98% | 4378-13-6
Brand: J&K Chemical
SKU: JKB12168_1_G
Price: 35.0 USD
Availability: OutOfStock

Cat. No JKB12168_1_G

Vendor: 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%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Prospects for the structure‒function evolution of SARS-CoV-2 main protease inhibitors

Ligand-based and structure-based studies to develop predictive models for SARS-CoV-2 main protease inhibitors through the 3d-qsar.com portal

Incorporation of Azide and Alkyne Functionalities into Peptides

Three-Component Reaction of Ketones, Amines, and Aldehydes via Enamine Catalysis

Development of an Amino Acid/Hydroxy Oxime Dual Catalyst System for Highly Stereoselective Direct Asymmetric Aldol Reactions in the Presence of Water