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You Searched For: Oxazolidine-4-carboxylic+acid+hydrochloride


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Oxazolidine-4-carboxylic acid hydrochloride 95%

Supplier: Ambeed
Description: Oxazolidine-4-carboxylic acid hydrochloride, Purity: 95%, CAS number: 1219384-60-7, Appearance: Solid, Storage: Inert atmosphere, Room Temperature, Size: 1G

Image Unavailable-102845-516

Methyl (4S)-2-oxo-3-piperidin-4-yl-1,3-oxazolidine-4-carboxylate hydrochloride ≥97%

Catalog Number: (102845-516)
Supplier: Matrix Scientific
Description: Methyl (4S)-2-oxo-3-piperidin-4-yl-1,3-oxazolidine-4-carboxylate hydrochloride ≥97%
Image Unavailable-76219-370

(4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid ≥98.0% (by GC, titration analysis)

Catalog Number: (76219-370)
Supplier: TCI America
Description: (4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-carboxylic Acid, Purity: >98.0%(GC)(T), CAS: 143527-70-2, Molecular Formula: C17H23NO5, Molecular Weight: 321.37, Size: 200MG
Image Unavailable-76995-094

(4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid 95%

Supplier: Ambeed
Description: (4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid 95%

Image Unavailable-TCB5657-5G

tert-Butyl (S)-4-(Hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate ≥97.0% (by GC)

Supplier: TCI America
Description: tert-Butyl (S)-4-(Hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate ≥97.0% (by GC)

New Product

Product Image-TS42635-0050

Methyl (R)-(+)-3-boc-2,2-dimethyl-4-oxazolidinecarboxylate 95%

Supplier: Thermo Scientific Chemicals
Description: Methyl (R)-(+)-3-boc-2,2-dimethyl-4-oxazolidinecarboxylate 95%

Image Unavailable-102526-414

(4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid ≥95%

Supplier: Matrix Scientific
Description: (4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid ≥95%

Image Unavailable-76990-894

Methyl (R)-(+)-3-boc-2,2-dimethyl-4-oxazolidinecarboxylate 97%

Supplier: Ambeed
Description: Methyl (R)-(+)-3-boc-2,2-dimethyl-4-oxazolidinecarboxylate 97%

New Product

Image Unavailable-76219-588

Methyl (R)-(+)-3-boc-2,2-dimethyl-4-oxazolidinecarboxylate ≥96.0% (by GC)

Supplier: TCI America
Description: (R)-(+)-3-(tert-Butoxycarbonyl)-4-methoxycarbonyl-2,2-dimethyl-1,3-oxazolidine, >96%, CAS: 95715-86-9, MF: C12H21NO5, MW: 259.30, Synonyms: (R)-(+)-3-Boc-4-methoxycarbonyl-2,2-dimethyl-1,3-oxazolidine, Size: 1G

Product Image-TS37089-0010

(R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde 95%

Catalog Number: (TS37089-0010)
Supplier: Thermo Scientific Chemicals
Description: (R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde 95%
Image Unavailable-77111-884

(R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde 97%

Supplier: Ambeed
Description: (R)-tert-Butyl 4-formyl-2,2-dimethyloxazolidine-3-carboxylate, Purity: 97%, CAS Number: 95715-87-0, Appearance: Liquid or Solid or Semi-solid or lump, Storage: Inert atmosphere, 2-8 deg C, Size: 100mg

Image Unavailable-B-3920.0005BA

Fmoc-Phe-Ser(Psi(Me,Me)pro)-OH

Catalog Number: (B-3920.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
Image Unavailable-B-3535.0005BA

Fmoc-Ala-Thr(Psi(Me,Me)pro)-OH

Catalog Number: (B-3535.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
Image Unavailable-B-3935.0005BA

Fmoc-Ser(tBu)-Ser(Psi(Me,Me)pro)-OH

Catalog Number: (B-3935.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
Image Unavailable-B-3540.0005BA

Fmoc-Leu-Ser(Psi(Me,Me)pro)-OH

Catalog Number: (B-3540.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
Image Unavailable-B-3910.0005BA

Fmoc-Ile-Ser(Psi(Me,Me)pro)-OH

Catalog Number: (B-3910.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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