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| Product | Description | |
|---|---|---|
| 2-Hydroxy-2-azaadamantane | Oxidation Organocatalysts. Alternative Names: MFCD27976826; 2-Azaadamantane-2-ol; BCJCJALHNXSXKE-UHFFFAOYSA-N; AZADOL(regR); AKOS026671304; 2-Hydroxy-2-azaadamantane. CAS No. 1155843-79-0. Molecular formula: C9H15NO. Mole weight: 153.225g/mol. IUPACName: 2-hydroxy-2-azatricyclo[3.3.1.13,7]decane. Canonical SMILES: C1C2CC3CC1CC(C2)N3O. Catalog: ACM1155843790. |  |
| 1-Phenylethane-1,2-diol | 1-Phenylethane-1,2-diol (Styrene Glycol) is a benzyl diol compound, which is the major metabolite of Styrene. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Styrene Glycol. CAS No. 93-56-1. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-W015788. |  |
| (R)-(-)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate, min. 98% [(R)-TiPSY] | A chiral phosphoric acid catalyst providing a convenient strategy for the enantioselective construction of protected primary amines and a highly stereoselective method for the reductive amination of heterocyclic amines. Chiral phosphoric acid used for the enantioselective Biginelli and Biginelli-like reactions. Chiral phosphoric acid organocatalyst used in the asymmetric, three-component Povarov reaction involving 2-hydroxystyrenes. An efficient method to access structurally diverse cis-disubstituted tetrahydroquinolines in high stereoselectivities of up to >99:1 dr and 97% ee. A gold/chiral phosphoric acid catalyst used for the highly stereoselective, three-component reaction of salicylaldehydes, anilines, and alkynols to give aromatic spiroacetals in high yields and stereoselectivities. The first highly enantioselective catalytic protocol for the reductive coupling of ketones and hydrozones. Reagent-controlled regioselectivity enabled by dual activation. Group: Organic phosphine compounds. Alternative Names: (S)-(+)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate; RD-0080; (11bR)-4-Hydroxy-2,6-bis(triphenylsilyl)dinaphtho-[2,1-d:1 inverted exclamation marka,2 inverted exclamation markaf]-1,3,2-dioxaphosphepin 4-oxide; Carreira SALDIPAC Ligand; (R)-(-)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogen phospÂ… | |
| Tempo | Tempo is a nitric oxide radical and a selective scavenger of ROS in mitochondria. Tempo is also an organocatalyst that disproportionates superoxide and oxidizes primary alcohols to aldehydes in a catalytic cycle. Tempo has mutagenic and antioxidant effects and can induce DNA strand breaks. Tempo also exerts cytotoxic and mutagenic properties in mouse lymphoma cells [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2564-83-2. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-W001187. | |
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