A series of novel aromatic sulfonamide derivatives (1–7) were synthesized and characterized by elemental analyses, FT-IR, 1 H NMR, 13 C NMR, and LC/MS techniques. The compounds' quantum mechanical descriptors, surface area, and molecular volume were calculated.
The Benzenesulfonyl fluoride, 3-chloro- molecule contains a total of 15 bond(s) There are 11 non-H bond(s), 8 multiple bond(s), 1 rotatable bond(s), 2 double bond(s), 6 aromatic bond(s), 1 six-membered ring(s) and 1 sulfone(s). Images of the chemical structure of Benzenesulfonyl fluoride, 3-chloro- are given below:
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The general structure for a hydrazide is (R 1 =O)R 2-N-N-R 3 R 4. Hydrazide derivatives have been reported to possess anticonvulsant, antioxidant, hormone antagonist, analgesic, anti-inflammatory, antiplatelet, antimalarial, antimicrobial, antimycobacterial, antitumor, vasodilator, antiviral and antitrypanosomal activities.
Substituted aromatic heterocyclic sulfonyl hydrazone compounds 4721 productive source of afflatus for medicinal chem-ists for many years due to their diverse inhibitory activities8. A recent research of flubiprofen ester hydrazide derivatives became much more attrac-tive and promising for the devise of anticancer agents.
Download Citation on ResearchGate | Influence of the Molecular Structure of H Complexes of Dialkyl Dihydrogen Benzophenonetetracarboxylates with Aromatic Diamines on the Viscosity of Their Melts ...
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Chemicals Delisted December 13, 2013 as Known to the State of California to Cause Reproductive Toxicity: tert‑amyl methyl ether, 2-ethylhexanoic acid, ethyl-tert-butyl ether, p,p'‑oxybis(benzenesulfonyl hydrazide) and 1,3,5-triglycidyl-s-triazinetrione
Advanced Search Structure Search. Analytical & Labware ... L19466 Benzenesulfonyl hydrazide, polymer-supported, 1.8-2.2 mmol/g on polystyrene . CAS Number.
exposure to p,p'-Oxybis (Benzene Sulfonyl Hydrazide. * Eye wash fountains should be provided in the immediate work area for emergency use. * On skin contact with p,p'-Oxybis (Benzenesulfonyl Hydrazide), immediately wash or shower to remove the chemical. At the end of the workshift, wash any areas of the body that may have contacted p,p ...
Applications 4,4′-Oxybis(benzenesulfonyl hydrazide) is an organic hydrazide used as a blowing agent for sponge rubber and expanded plastics. Used as an additive to polymers to make sponge rubber cosmetic puffs, electrostatographic toners, buoyant seats, insulation and packing materials, adhesives, sealants, and leather substitutes.
DIPHENYLOXIDE-4,4'-DISULFOHYDRAZIDE is an azide. Azo, diazo, azido compounds can detonate. This applies in particular to organic azides that have been sensitized by the addition of metal salts or strong acids.
Hydrazide is an acyl hydrazine. Acyl (-CO) is an organic radical formed by removal of a hydroxyl group from an organic acid (carboxyl group). Benzenesulfonyl Hydrazide is a foaming agent for rubbers and plastics such as PVC, EVA, polyolefin, polystyrene products.
Commercially available homobifunctional hydrazide compounds (i.e., those which have a hydrazide group at each end) include carbohydrazide (MW 90.1) and adipic acid dihydrazide (ADH, MW 174.2). These bis-hydrazide compounds could be used in a single reaction to crosslink and polymerize prepared (aldehyde-containing) sugars or polysaccharides ...
Benzenesulfonyl hydrazide 98% Synonym: BSH, Benzenesulfonylhydrazine, Porofor BSH CAS Number 80-17-1. Linear Formula C 6 H 5 SO 2 NHNH 2. Molecular Weight 172.20 . Beilstein/REAXYS Number 640079 . EC Number 201-255-2. MDL number MFCD00007583. PubChem Substance ID 24891736
The additive essential for the natural rubber foam was the benzenesulfonyl hydrazide (BSH) blowing agent. The molecular formula of the BSH blowing agent is C 6 H 8 N 2 O 2 S. It was used to change the cell structure of natural rubber in this work. The decomposition temperature of the BSH blowing agent was 105 °C at 120 cm 3 /g gas evolutions.
Particulate-phase p,p'-oxybis(benzenesulfonyl hydrazide) will be removed from the atmosphere by wet or dry deposition. p,p'-Oxybis(benzenesulfonyl hydrazide) does not contain chromophores that absorb at wavelengths >290 nm, and therefore is not expected to be susceptible to direct photolysis by sunlight.
Visit ChemicalBook To find more 4,4'-Oxybis(benzenesulfonyl hydrazide)(80-51-3) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes.
80-51-3 - NBOCQTNZUPTTEI-UHFFFAOYSA-N - p,p'-Oxybis(benzenesulfonyl hydrazide) - Similar structures search, synonyms, formulas, resource links, and other chemical information.
This paper describes the synthesis, self-assembly, and characterization of a new class of highly stable hydrazide-based quadruply hydrogen-bonded heterodimers. All of the hydrazide-derived heterodimers possess the complementary ADDA−DAAD hydrogen-bonding sequences.
Sulfonyl halide groups occur when a sulfonyl functional group is singly bonded to a halogen atom.They have the general formula RSO 2 X where X is a halogen. The stability of sulfonyl halides decreases in the order fluorides > chlorides > bromides > iodides, all four types being well known.
Hydrazide is an acyl hydrazine. Acyl (-CO) is an organic radical formed by removal of a hydroxyl group from an organic acid (carboxyl group). p-Toluenesulfonyl Hydrazide is a foaming agent for rubbers and plastics such as PVC, EVA, polyolefin, polystyrene products.
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