Boc-γ-Abu-OH

Name: Boc-γ-Abu-OH | 57294-38-9
Brand: US-CATO
SKU: S57CPTD788026_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD788026_10_MG

Vendor: US-CATO

Product Information

Product Name

Boc-γ-Abu-OH

Brand Name

US-CATO

Product Number

CPTD788026

CAS

57294-38-9

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

294894

IUPAC Name

4-(2-methylpropan-2-yl)oxycarbonylaminobutanoic acid

InChI Key

HIDJWBGOQFTDLU-UHFFFAOYSA-N

SMILES

CC(C)(C)OC(=O)NCCCC(=O)O

References Data Source From Pubchem

Bisulfite-mediated base-free decarboxylative carbonylsulfination of alkenes: access to β-keto sultines

Publication Name: Science China Chemistry

Publication Date: 2024-09-24

DOI: 10.1007/s11426-024-2210-2

Accurate de novo design of heterochiral protein–protein interactions

Publication Name: Cell Research

Publication Date: 2024-08-14

DOI: 10.1038/s41422-024-01014-2

Synthesis and Evaluation of the Antimicrobial Activity of Cationic Amphiphiles Based on Bivalent Diethylenetriamine Derivatives

Publication Name: Pharmaceutical Chemistry Journal

Publication Date: 2023-03

DOI: 10.1007/s11094-023-02834-z

A β-Lactone for Covalent Inhibition of KRAS G12S

Publication Name: Synfacts

Publication Date: 2022-09-20

DOI: 10.1055/s-0041-1738592

Removable Backbone Modification (RBM) Strategy for the Chemical Synthesis of Hydrophobic Peptides/Proteins

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2022-06-28

DOI: 10.1007/978-1-0716-2489-0_16

Boc-γ-Abu-OH

Product Information

General Information

References Data Source From Pubchem

Bisulfite-mediated base-free decarboxylative carbonylsulfination of alkenes: access to β-keto sultines

Accurate de novo design of heterochiral protein–protein interactions

Synthesis and Evaluation of the Antimicrobial Activity of Cationic Amphiphiles Based on Bivalent Diethylenetriamine Derivatives

A β-Lactone for Covalent Inhibition of KRAS G12S

Removable Backbone Modification (RBM) Strategy for the Chemical Synthesis of Hydrophobic Peptides/Proteins

Boc-γ-Abu-OH

Mycophenolate Mofetil EP Impurity H

Mycophenolate Mofetil

Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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Boc-γ-Abu-OH

Product Information

General Information

References Data Source From Pubchem

Bisulfite-mediated base-free decarboxylative carbonylsulfination of alkenes: access to β-keto sultines

Accurate de novo design of heterochiral protein–protein interactions

Synthesis and Evaluation of the Antimicrobial Activity of Cationic Amphiphiles Based on Bivalent Diethylenetriamine Derivatives

A β-Lactone for Covalent Inhibition of KRAS G12S

Removable Backbone Modification (RBM) Strategy for the Chemical Synthesis of Hydrophobic Peptides/Proteins

Boc-γ-Abu-OH

Related Product

Mycophenolate Mofetil EP Impurity H

Mycophenolate Mofetil

Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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