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| Product | Description | |
|---|---|---|
| Iodobenzene diacetate | 100g Pack Size. Group: Building Blocks, Organics. Formula: C10H11IO4. CAS No. 3240-34-4. Prepack ID 62191868-100g. Molecular Weight 322.1. See USA prepack pricing. |  |
| Iodobenzene diacetate | 25g Pack Size. Group: Building Blocks, Organics. Formula: C10H11IO4. CAS No. 3240-34-4. Prepack ID 62191868-25g. Molecular Weight 322.1. See USA prepack pricing. | |
| Iodobenzene Diacetate | Iodobenzene Diacetate. CAS No: 3240-34-4 |  Sarchem Laboratories New Jersey NJ |
| Iodobenzene 1,1-diacetate | Iodobenzene 1,1-diacetate. Group: Biochemicals. Alternative Names: Iodosobenzene diacetate; Bis (acetoxy)iodobenzene. Grades: Highly Purified. CAS No. 3240-34-4. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. Molecular Formula: C10H11IO4. US Biological Life Sciences. |  Worldwide |
| (Diacetoxyiodo)benzene | (Diacetoxyiodo)benzene is a hypervalent iodine reagent that is used in conjunction with catalytic amount of sodium azide in acetonitrile, which enables oxidative decarboxylation of 2-aryl carboxylic acid into the corresponding aldehydes, ketones and nitriles. Group: Biochemicals. Alternative Names: (Dihydroxyiodo) benzene; (Diacetoxyiodo) benzene; BAIB; Bis (acetato)phenyliodine; Bis(acetato-κO)phenyliodine; Diacetoxy (phenyl)iodine; Iodobenzene Diacetate; Iodophenyl Diacetate; Iodosobenzene Diacetate; Iodosylbenzene Diacetate; NSC 226375; NSC 23801; PIDA; Phenyliodine Diacetate; Phenyliodine(III) Diacetate; Phenyliodo Diacetate; Phenyliodonium Diacetate; Phenyliodoso Acetate; Phenyliodoso Diacetate; Phenyliodosyl Diacetate; [Bis (acetoxy)iodo]benzene; Iodosodiacetate Benzene. Grades: Highly Purified. CAS No. 3240-34-4. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| (Diacetoxyiodo)benzene | Synonyms: Iodobenzene diacetate; Iodosobenzene diacetate; Phenyliodo diacetate. CAS No. 3240-34-4. Molecular formula: C10H11IO4. Mole weight: 322.10. |  |
| Polystyrene iodosoacetate | Polystyrene iodosoacetate. Group: Polymers. Alternative Names: POLYSTYRENE IODOSOACETATE; POLY[4-(DIACETOXYIODO)STYRENE]; PolystyreneIodosoacete; Poly[4-(diacetoxyiodo)styrene], Loading: 1~5MMol/G; Bis(acetato-O)(4-ethenylphenyl)iodine homopolymer; polystyrene supported iodobenzene diacetate; Polystyrene. CAS No. 36290-94-5. Mole weight: (C12< / sub>H13< / sub>IO4< / sub>) n. 96%. |  |
| TEMPO | (2,2,6,6-Tetramethylpiperidin-1-yl)oxyl or (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl, commonly known as TEMPO, is a chemical compound with the formula (CH2)3(CMe2)2NO. This heterocyclic compound is a red-orange, sublimable solid. As a stable radical, it has applications in chemistry and biochemistry. TEMPO was discovered by Lebedev and Kazarnowskii in 1960. It is prepared by oxidation of 2,2,6,6-tetramethylpiperidine. TEMPO is widely used as a radical marker, as a structural probe for biological systems in conjunction with electron spin resonance spectroscopy, as a reagent in organic synthesis, and as a mediator in controlled radical polymerization. The stability of this radical is attributed to the resonance provided by non-bonding electrons on the nitrogen atom, which form a 2c3e (half-) bond between nitrogen and oxygen, and hyperconjugative ability. Additional stability arises from the steric protection provided by the four methyl groups adjacent to the nitroxyl group; however, the methyl groups prevent a double bond occurring between either carbon adjacent to nitrogen. The stability of the radical is also indicated by the weakness of the O-H bond in the hydrogenated derivative TEMPO-H. With an O-H bond dissociation energy of about 70kcal/mol, this bond is about 30% weaker than a typical O-H bond. Uses: Contact reaction oxidant for iodobenzene diacetyl to oxidize nerol to generate neral. in summary, copper/tempo is used for thÂ… |  |
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