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Poly(vinylsulfonicacid, sodium salt) is a polymer that consists of repeating units of vinylsulfonicacid monomers, where each vinylsulfonicacid unit is neutralized with a sodium cation (Na+). Poly(vinylsulfonicacid, sodium salt) is an example of a polyelectrolyte, which is a type of polymer that contains ionizable groups along its chain. The presence of sulfonicacid groups (-SO3H) in this polymer provides it with strong acidic properties. However, when the polymer is neutralized with sodium ions, it becomes water-soluble and exhibits enhanced solubility and stability in aqueous solutions. Uses: Poly(vinylsulfonicacid, sodium salt) (pvsa) can be used: in the preparation of superabsorbent semi-ipn (interpenetrating polymer network) hydrogel. as a solid electrolyte for proton conduction in the fabrication of an all-solid-supercapacitor. as a crystallization controlling agent in the preparation of high-quality crystals of porous coordination polymers(cp). pvsa regulates not only the size and structure of the crystals but also their preference orientation, resulting in cp channel alignment in the bulk powdery state. Alternative Names: PVSA. CAS No. 9002-97-5. Molecular formula: (C2H3NaO3S)n. Mole weight: 130.098. Appearance: Liquid. Purity: 0.75. Canonical SMILES: [Na]OS(=O)(=O)C=C. Density: 1.267 g/mL at 25ºC. Catalog: ACM9002975.
Effective ligand for the Pd-catalyzed arylation of pyrazoles, indazoles and amino heterocycles. Ligand used in the Pd-catalyzed synthesis of phenols from aryl halides and KOH. Ligand used in the Pd-catalyzed of benzoic acids from aryl halides and CO2. Ligand used in the Pd-catalyzed trifluoromethylation of vinyl sulfonates. Ligand used in the Pd-catalyzed arylation of nitroacetates. Ligand used in the Pd-catalyzed Suzuki-Miyaura cross-coupling of allylboronates and aryl halides. Ligand used in the Pd-catalyzed cyanation of (hetero)arylchlorides and bromides. Ligand used in the Pd-catalyzed C-N cross coupling of sulfinamides and aryl halides. Ligand used in the Pd-catalyzed arylation of cyanamides. Group: Organic phosphine compounds. Alternative Names: DTXSID70469549; t-Bu XPhos; FT-0689983; TC-121258; 2-Di-tert-butylphosphino-2 inverted exclamation marka,4 inverted exclamation marka,6 inverted exclamation marka-triisopropylbiphenyl; tBuXPhos; ditert-butyl-[2-(2,4,6-triisopropylphenyl)phenyl]phosphane; ZINC56961724; 2-Di-tert-butylphosphino-2',4',6'-triisopropylbiphenyl; 2-(di-tert-butylphosphino)-2', 4',6'-triisopropylbiphenyl. CAS No. 564483-19-8. Molecular formula: C29H45P. Mole weight: 424.653g/mol. IUPACName: ditert-butyl-[2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane. Canonical SMILES: CC (C)C1=CC (=C (C (=C1)C (C)C)C2=CC=CC=C2P (C (C) (C)C)C (C) (C)C)C (C)C. Catalog: ACM5644
3-?[[ (4-?Methylphenyl) ?sulfonyl]?oxy]?-butanoic Acid Ethyl Ester is an intermediate in synthesizing 2-Desethyl-2-vinyl Simvastatin (D289830), a Simvastatin (S485000) impurity. Group: Biochemicals. Grades: Highly Purified. CAS No. 316148-56-8. Pack Sizes: 100mg, 250mg. Molecular Formula: C15H22O5S. US Biological Life Sciences.
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Recilisib
Recilisib, also known as ON 01210.Na, is a radioprotectant, which modifys cell cycle distribution patterns in cancer cells subjected to radiation therapy. It appears that Recilisib radioprotective mechanisms involve prevention of p53-dependent and independent radiation-induced apoptosis. It can activate AKT, PI3K activities in cells. Synonyms: ON 01210; (E)-4-(2-((4-Chlorobenzyl)sulfonyl)vinyl)benzoic acid; ON-01210. Grades: >98%. CAS No. 334969-03-8. Molecular formula: C16H13ClO4S. Mole weight: 336.79.
tert-Butyl Vinylsulfonylcarbamate
tert-Butyl Vinyl sulfonyl carbamate. Group: Biochemicals. Alternative Names: (Ethenylsulfonyl) carbamic Acid 1,1-Dimethylethyl Ester. Grades: Highly Purified. CAS No. 452341-63-8. Pack Sizes: 500mg. Molecular Formula: C7H13NO4S, Molecular Weight: 207.25. US Biological Life Sciences.
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