You Searched For: 2-Chloro-3-pyridineboronic+acid+pinacol+ester


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Supplier: Thermo Fisher Scientific
Description: 1,4-Dibromo-2,5-difluorobenzene ≥98%
Catalog Number: (APOSPC302763-1G)
Supplier: Apollo Scientific
Description: 6-Chloro-2,3-difluorobenzoyl chloride 98%
UOM: 1 * 1 g


Supplier: Thermo Fisher Scientific
Description: PPDT2FBT (PCE9.3), Organic Photovoltaics (OPV) reagent

Supplier: Apollo Scientific
Description: see: Org. Synth., 75, 201 (1997), a discussion of lithiation, including dibenzyne formation.

Supplier: Apollo Scientific
Description: 2-Chloro-3,6-difluoroanisole 98%

Supplier: Apollo Scientific
Description: 5,7-Difluoroindole

Supplier: Apollo Scientific
Description: 2-Bromo-3,6-difluorobenzeneboronic acid 95%

Supplier: Apollo Scientific
Description: 2-Chloro-1,4-difluorobenzene 98%

Supplier: Thermo Fisher Scientific
Description: 2-Bromo-1,4-difluorobenzene ≥98%
Supplier: Apollo Scientific
Description: 2-Bromo-1,4-difluorobenzene 98%

Supplier: Apollo Scientific
Description: 2-Chloro-3,6-difluorophenol 97%

Supplier: Merck
Description: α-Chymotrypsin is a serine peptidase and has 241 amino acid residues contained in three polypeptide chains (A chain-13 residues, B chain-131 residues, and C chain-97 residues) linked by disulfide bridges. Molecular weight of this enzyme is found to be 25 kDa. Its pI is 8,75. It selectively hydrolyses peptide bonds on the C-terminal side of tyrosine, phenylalanine, tryptophan, and leucine. Ca²⁺ activates and stabilizes the enzyme. The enzyme is inhibited by diisopropyl fluorophosphate (DFP), phenylmethanesulfonyl fluoride (PMSF), N-p-tosyl-L-phenylalanine chloromethyl ketone (TPCK), chymostatin, aprotinin, α1-antitrypsin, α2-macroglobulin, 10 mM Cu²⁺ and Hg²⁺.A serine protease that hydrolyzes peptide bonds with aromatic or large hydrophobic side chains (Tyr, Trp, Phe, Met, Leu) on the carboxyl end of the bond.

Catalog Number: (786-13)
Supplier: G-Biosciences
Description: SG-Chymotrypsin™ is a serine endopeptidase, which predominantly cleaves peptide bonds on the carboxy side of tyrosine, phenylalanine and tryptophan. In addition, chymotrypsin has a low catalytic activity against the carboxy side of leucine, methionine, alanine, aspartic and glutamic acids. It is therefore recommended to always use the shortest digestion time possible.
UOM: 1 * 2 items


Catalog Number: (MAYBHAN00007.1)
Supplier: Thermo Scientific
Description: 1-Bromo-2,5-difluoro-4-nitrobenzene
UOM: 1 * 1 g


Supplier: Thermo Scientific
Description: 1,4-Difluoro-2-nitrobenzene

Catalog Number: (SIAL196622-25G)
Supplier: Merck
Description: 1,4-Difluoro-2-nitrobenzene, Sigma-Aldrich®
UOM: 1 * 25 g


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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 +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
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