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Catalog Number: (ALA121934-1G)
Supplier: ALADDIN SCIENTIFIC
Description: 2992793

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Catalog Number: (ALA121492-1G)
Supplier: ALADDIN SCIENTIFIC
Description: 2992793

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Supplier: ALADDIN SCIENTIFIC
Description: Aldehyde allylation reagent, the catalyst of this reaction is chiral Lewis acid and Ytterbium(III) trifluoromethanesulfonate. Catalyzed by tetrakis(triphenylphosphine)palladium (0) (product number 216666), it reacts with iodoquinone 4 and allyl acetate. Used in the efficient allylation reaction of aldehydes and trichloro-1,3,5-triazene to produce high allyl alcohol.

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Supplier: ALADDIN SCIENTIFIC
Description: 2992793

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Supplier: ALADDIN SCIENTIFIC
Description: 2992793

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Supplier: ALADDIN SCIENTIFIC
Description: 2992793

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Supplier: ALADDIN SCIENTIFIC
Description: Application:5-Amino-3-methyl-isothiazole hydrochloride may be used in chemical synthesis studies.Used for pharmacological studies as a precursor for:1.MMP12 inhibitors2.Aurora kinase inhibitors3.N-Heterocyclic indolyl glyoxylamides as anticancer agents.

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Supplier: ALADDIN SCIENTIFIC
Description: (1S,2R)-(+)-2-Amino-1,2-diphenylethanol can be used:· To prepare vanadium(V) Schiff base complexes, which are used as catalysts in the oxidation of sulfides and olefins. · To prepare chiral selectors, which are immobilized on aminated silica gel, applicable as chiral stationary phase in HPLC. · To immobilize on the frame of α-zirconium phosphate to yield layered zirconium phosphonates, which are used in the heterogeneous catalysis. · As a chiral auxiliary in the preparation of homopropargylic alcohols from aliphatic and aromatic aldehydes.

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Supplier: ALADDIN SCIENTIFIC
Description: Ambrisentan is a selective ET type A receptor (ETAR) antagonist.

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Supplier: ALADDIN SCIENTIFIC
Description: 2992793

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Supplier: ALADDIN SCIENTIFIC
Description: Synthesis of tridentate Schiff base ligand and novel non-metallocene catalysts with phenoxy-imine ligands.

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Supplier: ALADDIN SCIENTIFIC
Description: Amylose is a polyglucose polysaccharide which together with amylopectin makes starch(s). The glucosidic bonds of amylopectin are α-1,4 linkages. Amylose is used to identify, differentiate and characterize amylase(s). Amylose is used as a thickening agent, a gelling agent and emulsion stabilizer. Amylose is used in the preparation of films and membranes with potential use in drug A substrate for serum amylase.Application:

Amylose in potato has been used as a standard to determine the apparent amylose content (AAC) of rice starch by iodine-binding colorimetry.

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Supplier: ALADDIN SCIENTIFIC
Description: 2992793

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Supplier: ALADDIN SCIENTIFIC
Description: Usually used in the synthesis of 2,6-difluoro-N-(3-methoxy-1H-pyrazolo[3,4-b]pyridine-5-yl)-3-(propylsulfonamidio)benzamide and heteroaromatic 3-hydroxy-5,6-diphenylpyrazolo[3,4-b]pyridines.

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Supplier: ALADDIN SCIENTIFIC
Description: 2-Amino-5-chlorophenol can be synthesized from 2-chloro-5-nitrophenol via reduction. It can also be obtained from 1-chloro-4-nitrobenzene by using a bacterial strain LW1. 2-Amino-5-chlorophenol participates in the condensation reaction with acetylferrocene to afford ferrocenyl Schiff bases bearing a phenol group.2-Amino-5-chlorophenol may be used to synthesize 2-amino-5-chloromuconic semialdehyde and benzoxazole derivatives.

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Catalog Number: (ALA169216-1G)
Supplier: ALADDIN SCIENTIFIC
Description: 2992793

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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.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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