H-Thr(tBu)-OH

Name: H-Thr(tBu)-OH | 4378-13-6
Brand: US-CATO
SKU: S57CPTD787843_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD787843_10_MG

Vendor: US-CATO

Product Information

Product Name

H-Thr(tBu)-OH

Brand Name

US-CATO

Product Number

CPTD787843

CAS

4378-13-6

Certificate of Analysis (COA)

COA not found

General Information

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

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

H-Thr(tBu)-OH

Product Information

General 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

H-Thr(tBu)-OH

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H-Thr(tBu)-OH

Product Information

General 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

H-Thr(tBu)-OH

Related Product

Mycophenolate Mofetil EP Impurity H

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Flurbiprofen Impurity 21 (Mixture of Diastereomers)

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H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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