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You Searched For: Boc-S-trityl-L-penicillamine


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N-(tert-Butoxycarbonyl)-D-glutamic acid ≥97.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 34404-28-9
MDL Number: MFCD00190790
Molecular Formula: C10H17NO6
Molecular Weight: 247.25
Purity/Analysis Method: >97.0% (HPLC,T)
Form: Crystal
Melting point (°C): 108
Specific rotation [a]20/D: 14 deg (C=1, MeOH)

SDS Certificates

Image Unavailable-TCB5132-1G

4-(tert-Butoxycarbonyl)phenylboronic acid pinacol ester ≥97.0% (by GC, titration analysis)

Supplier: TCI America
Description: Tert-Butyl 4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Benzoate, Purity: >97.0%(GC)(T), Cas no: 850568-72-8, Molecular formula : C17H25BO4, Synonyms: 4-Boc-phenylboronic Acid Pinacol Ester, Size: 5G

Image Unavailable-TCB3249-25G

cis-4-(tert-Butoxycarbonylamino)cyclohexanecarboxylic acid ≥98.0% (by GC, titration analysis)

Supplier: TCI America
Description: CAS Number: 53292-90-3
MDL Number: MFCD01862294
Molecular Formula: C12H21NO4
Molecular Weight: 243.30
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 169

SDS Certificates

Image Unavailable-TCB3052-1G

N-(tert-Butoxycarbonyl)-2,2-dimethyl-1,3-propanediamine ≥98.0% (by GC, titration analysis)

Catalog Number: (TCB3052-1G)
Supplier: TCI America
Description: CAS Number: 292606-35-0
MDL Number: MFCD01076212
Molecular Formula: C10H22N2O2
Molecular Weight: 202.30
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 74

Certificates


Image Unavailable-TCB3478-1G

(1R,2S)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine ≥98.0% (by GC, titration analysis)

Supplier: TCI America
Description: CAS Number: 364385-54-6
MDL Number: MFCD09952106
Molecular Formula: C11H22N2O2
Molecular Weight: 214.31
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Specific rotation [a]20/D: 5.0 deg (C=1, CH2Cl2)
Storage Temperature: 0-10°C

SDS Certificates

Image Unavailable-TCB3177-1G

(2S,4R)-1-(tert-Butoxycarbonyl)-4-fluoro-2-pyrrolidinecarboxylic acid ≥96.0% (by GC, titration analysis)

Supplier: TCI America
Description: CAS Number: 203866-14-2
MDL Number: MFCD06796085
Molecular Formula: C10H16FNO4
Molecular Weight: 233.24
Purity/Analysis Method: >96.0% (GC,T)
Form: Crystal
Melting point (°C): 116
Specific rotation [a]20/D: -69 deg (C=1, MeOH)

SDS

Image Unavailable-CAAAB22435-14

2-(tert-Butoxycarbonylthio)-4,6-dimethylpyrimidine 97%

Supplier: Thermo Scientific Chemicals
Description: 2-(tert-Butoxycarbonylthio)-4,6-dimethylpyrimidine 97%

Certificates

Image Unavailable-CA80050-798

Calbiochem® Caspase Inhibitor III

Supplier: MilliporeSigma
Description: A cell-permeable, irreversible, broad-spectrum caspase inhibitor.

Image Unavailable-TCA1172-25G

(3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidine ≥98.0% (by GC, titration analysis)

Supplier: TCI America
Description: CAS Number: 122536-76-9
MDL Number: MFCD00143194
Molecular Formula: C9H18N2O2
Molecular Weight: 186.26
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 78
Specific rotation [a]20/D: -20 deg (C=1, EtOH)

SDS Certificates

Image Unavailable-TCA2708-1G

tert-Butyl-6-aminopyridin-2-ylcarbamate ≥97.0% (by titrimetric analysis)

Supplier: TCI America
Description: CAS Number: 322690-31-3
MDL Number: MFCD09037865
Molecular Formula: C10H15N3O2
Molecular Weight: 209.25
Purity/Analysis Method: >97.0% (T)
Form: Crystal
Melting point (°C): 127

SDS

Image Unavailable-TCB3071-5G

Nε-(tert-butoxycarbonyl)-Nɑ-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-lysine ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 92122-45-7
MDL Number: MFCD00065660
Molecular Formula: C26H32N2O6
Molecular Weight: 468.55
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 130
Specific rotation [a]20/D: 2.2 deg (C=1, MeOH)
Storage Temperature: 0-10°C

SDS

Image Unavailable-B-3965.0001BA

Boc-Thr(Ile-Fmoc)-OH

Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.

Image Unavailable-B-3975.0005BA

Boc-Thr(Leu-Fmoc)-OH

Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.

Image Unavailable-B-3985.0001BA

Boc-Thr(Val-Fmoc)-OH

Catalog Number: (B-3985.0001BA)
Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.
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N-(tert-Butoxycarbonyl)-trans-4-hydroxy-L-prolinemethyl ester ≥95.0% (by GC)

Supplier: TCI America
Description: CAS Number: 74844-91-0
MDL Number: MFCD00076981
Molecular Formula: C11H19NO5
Molecular Weight: 245.28
Purity/Analysis Method: >95.0% (GC)
Form: Crystal
Boiling point (°C): 132
Melting point (°C): 96
Specific rotation [a]20/D: -79 deg (C=1, MeOH)

SDS

Image Unavailable-B-3930.0005BA

Fmoc-Lys(Boc)-Thr(Psi(Me,Me)pro)-OH

Catalog Number: (B-3930.0005BA)
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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