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2,2-Dimethyl-4-pentenoic+acid
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2,2-Dimethyl-4-pentenoic+acid
Supplier:
TCI America
Description:
CAS Number: 7685-44-1
MDL Number: MFCD00063103 Molecular Formula: C5H9NO2 Molecular Weight: 115.13 Purity/Analysis Method: >98.0% (HPLC) Form: Crystal Melting point (°C): 220 Storage Temperature: 0-10°C
Supplier:
ALADDIN SCIENTIFIC
Description:
α-Angelica lactone, a cyclic lactone that occurs naturally in tobacco, is generally used in tobacco flavoring.
Supplier:
AMBEED, INC
Description:
Boc-D-allyl-Gly-OH dicyclohexylammonium salt 97%
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041452-5G , MDL Number: MFCD01321012
Catalog Number:
(TCA1090-100G)
Supplier:
TCI America
Description:
CAS Number: 591-12-8
MDL Number: MFCD00005375 Molecular Formula: C5H6O2 Molecular Weight: 98.10 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Boiling point (°C): 56 Flash Point (°C): 68 Freezing point (°C): 16 Specific Gravity (20/20): 1.10
Supplier:
BeanTown Chemical
Description:
CAS: 21286-54-4; MDL No: MFCD00064156
UN No: UN3261; Haz Class: 8; Packing Group: II
Crystalline; Molecular Formula: C10H15ClO3S ; MW: 250.74
Melting Point: 65-67°
Optical Rotation: [α]22/D +33°, c = 1 in chloroform
Moisture Sensitive
Supplier:
Thermo Scientific Chemicals
Description:
1g CAS: 170899-08-8, MDL: MFCD01321012
Supplier:
AMBEED, INC
Description:
(1R)-(-)-Camphor-10-sulfonyl chloride 97%
Catalog Number:
(B-3925.0005BA)
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.
Supplier:
Bachem Americas
Description:
Allylglycine-containing peptides may be cleaved selectively at the amide bond between allylglycine and the subsequent amino acid with iodine. The lateral double bond allows selective modifications of a peptide e.g. via metathesis. Replacing cysteine residues by allylglycine allows to obtain carba-analogs of disulfide-bridged peptides.Educt for obtaining Fmoc-prenylglycine.
Catalog Number:
(76809-958)
Supplier:
AMBEED, INC
Description:
5-Methylfuran-2(3H)-one, Purity: 98%, CAS Number: 591-12-8, Appearance: Low-melting Solid or Semi-solid or liquid, Storage: Inert atmosphere, 2-8C, Size: 5G
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.
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.
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.
Catalog Number:
(B-3915.0005BA)
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
is still displayed and you need assistance, please call us at 1-800-932-5000.
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