Boc-Gln-OH, 98%

Name: Boc-Gln-OH, 98% | 13726-85-7
Brand: J&K Chemical
SKU: JKB10038_5_G
Price: 32.7 USD
Availability: OutOfStock

Cat. No JKB10038_5_G

Vendor: J&K Chemical

Product Information

Product Name

Boc-Gln-OH, 98%

Brand Name

J&K

Product Number

261599

CAS

13726-85-7

Molecular Formula

C10H18N2O5

Molecular Weight

246.26

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

Nα-(tert-Butoxycarbonyl)-L-glutamine
Boc-L-glutamine

PubChem CID

83687

IUPAC Name

(2S)-5-amino-2-(2-methylpropan-2-yl)oxycarbonylamino-5-oxopentanoic acid

InChI Key

VVNYDCGZZSTUBC-LURJTMIESA-N

SMILES

CC(C)(C)OC(=O)NC@@H(CCC(=O)N)C(=O)O

Properties

Melting Point

113-116

Optical Activity

-3.9° to -2.9° (C=2, EtoH)

Safety Information

Precautionary Statement

P262

References Data Source From Pubchem

Inverse Peptide Synthesis Using Transient Protected Amino Acids

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

Publication Date: 2025

DOI: 10.1007/978-1-0716-4562-8_21

A multi-step continuous flow synthesis of pomalidomide

Publication Name: Journal of Flow Chemistry

Publication Date: 2022-04-19

DOI: 10.1007/s41981-022-00223-3

An Improved Synthesis of β-Cyano-l-Alanine Esters and Amides

Publication Name: Synlett

Publication Date: 2015-09-30

DOI: 10.1055/s-0035-1560489

Biomimetic Affinity Ligands for Immunoglobulins Based on the Multicomponent Ugi Reaction

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

Publication Date: 2012

DOI: 10.1007/978-1-61779-349-3_5

Synthesis of Thalidomide

Publication Name: Topics in Heterocyclic Chemistry

Publication Date: 2007

DOI: 10.1007/7081_2007_057

Boc-Gln-OH, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Inverse Peptide Synthesis Using Transient Protected Amino Acids

A multi-step continuous flow synthesis of pomalidomide

An Improved Synthesis of β-Cyano-l-Alanine Esters and Amides

Biomimetic Affinity Ligands for Immunoglobulins Based on the Multicomponent Ugi Reaction

Synthesis of Thalidomide

Boc-Gln-OH, 98%

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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Boc-Gln-OH, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Inverse Peptide Synthesis Using Transient Protected Amino Acids

A multi-step continuous flow synthesis of pomalidomide

An Improved Synthesis of β-Cyano-l-Alanine Esters and Amides

Biomimetic Affinity Ligands for Immunoglobulins Based on the Multicomponent Ugi Reaction

Synthesis of Thalidomide

Boc-Gln-OH, 98%

Related Product

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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