Chemicals list & Research Gallery

1-Octene
CAS number: 111-66-0
1-octene appears as a colorless liquid. Flash point 70 °F. Insoluble in water and less dense (at about 6 lb / gal) than water. Hence floats on water. The alkene is classified as a higher olefin and alpha-olefin.
Phosphorus hydrides and the adducts from addition to 1-octene.
Phosphorus hydrides and the adducts from addition to 1-octene.
Order of reactivity of phosphorus hydrides to 1-octene.
Order of reactivity of phosphorus hydrides to 1-octene.
Heptanal
CAS number: 111-71-7
Heptanal is an n-alkanal resulting from the oxidation of the alcoholic hydroxy group of heptan-1-ol to the corresponding aldehyde.
Simplified scheme of the reaction of acetaldehyde and heptanal on a solid basic and acid catalyst.
Simplified scheme of the reaction of acetaldehyde and heptanal on a solid basic and acid catalyst.
Cross- and self-condensation from the carbanion of heptanal.
Cross- and self-condensation from the carbanion of heptanal.
Cross-condensation between the carbanion of acetaldehyde and heptanal.
Cross-condensation between the carbanion of acetaldehyde and heptanal.
Selectivity to 1 as a function of heptanal conversion in the reaction of acetaldehyde and heptanal at different reaction temperatures.
Selectivity to 1 as a function of heptanal conversion in the reaction of acetaldehyde and heptanal at different reaction temperatures.
Selectivity to 1 as a function of heptanal (A) and acetaldehyde (B) conversions in the reaction of acetaldehyde and heptanal at different acetaldehyde/heptanal molar ratios.
Selectivity to 1 as a function of heptanal (A) and acetaldehyde (B) conversions in the reaction of acetaldehyde and heptanal at different acetaldehyde/heptanal molar ratios.
1-Octanethiol
CAS number: 111-88-6
Octane-1-thiol is an alkanethiol that is octane substituted by a thiol group at position 1.
STm image of n-octanethiolates on Au(111) in the p(6×√3) arrangement (40 nm × 40 nm, -0.95 V, 37 pA). The gold substrate was immersed for 8 h in 0.1 m n-octanethiol solution in ethanol at 23 °C and stored under ambient conditions for 5 days before the image was recorded.
STm image of n-octanethiolates on Au(111) in the p(6×√3) arrangement (40 nm × 40 nm, -0.95 V, 37 pA). The gold substrate was immersed for 8 h in 0.1 m n-octanethiol solution in ethanol at 23 °C and stored under ambient conditions for 5 days before the image was recorded.
STm image of n-octanethiolates on Au(111) in the (√3×√3)-R30 arrangement (8 nm × 8 nm, -1 V, 16 pA). The gold substrate was immersed for 8 h in 0.1 m n-octanethiol solution in ethanol at 55 °C.
STm image of n-octanethiolates on Au(111) in the (√3×√3)-R30 arrangement (8 nm × 8 nm, -1 V, 16 pA). The gold substrate was immersed for 8 h in 0.1 m n-octanethiol solution in ethanol at 55 °C.
STm image of ligands 18 embedded in an n-octanethiolate matrix on Au(111) (33 nm × 33 nm, 1.2 V, 18 pA). The ligands appear as protrusions, and the height difference between the n-octanethiolates and the ligand 18 amounts to about 1.5-2.5 Å.
STm image of ligands 18 embedded in an n-octanethiolate matrix on Au(111) (33 nm × 33 nm, 1.2 V, 18 pA). The ligands appear as protrusions, and the height difference between the n-octanethiolates and the ligand 18 amounts to about 1.5-2.5 Å.
DIF-1
CAS number: 111050-72-7
DIF-1 is a novel chlorinated alkyl phenone which induces differentiation of prestalk cells in Dictyostelium discoideum. DIF-1 is required for slug migration and specifies the anterior-like cells forming the basal disc and much of the lower cup.
Synthetic Routs to DIF Derivatives
Synthetic Routs to DIF Derivatives
Effects of DIF Derivatives on Cell Growth in HeLa, LM8, and 3T3-L1 Cells
Effects of DIF Derivatives on Cell Growth in HeLa, LM8, and 3T3-L1 Cells
Effects of DIF Derivatives on Infection and Growth of T. cruzi
Effects of DIF Derivatives on Infection and Growth of T. cruzi
Effects of DIF Derivatives on IL-2 Production in Jurkat T Cells
Effects of DIF Derivatives on IL-2 Production in Jurkat T Cells
Effects of DIF Derivatives on Glucose Consumption in 3T3-L1 Cells
Effects of DIF Derivatives on Glucose Consumption in 3T3-L1 Cells
Oxadiazoles
CAS number: 11120-54-0
An oxadiazole is defined as a doubly unsaturated 5-membered ring composed of two carbons, two nitrogens, and one oxygen atom. Oxadiazoles are a class of antibacterials discovered by in silico docking and scoring of compounds against the X-ray structure of a penicillin-binding protein.
Synthesis of oxadiazole from benzil dioxime.
Synthesis of oxadiazole from benzil dioxime.
Rose Bengal
CAS number: 11121-48-5
Rose bengal is an organic potassium salt that is the dipotassium salt of 2,3,4,5-tetrachloro-6-(2,4,5,7-tetraiodo-6-hydroxy-3-oxoxanthen-9-yl)benzoic acid. It has a role as a fluorochrome and a histological dye. It is a xanthene dye and an organic potassium salt. It contains a rose bengal(2-). It is functionally related to a fluorescin.
(a) Reichardt’s dye in water in the presence and absence of 5. (b) Rose Bengal (RB) in toluene in the presence and absence of 5.
(a) Reichardt’s dye in water in the presence and absence of 5. (b) Rose Bengal (RB) in toluene in the presence and absence of 5.
Threonine Phosphate
CAS number: 1114-81-4
O-phospho-L-threonine is a L-threonine derivative phosphorylated at the side-chain hydroxy function. It has a role as an Escherichia coli metabolite. It is a L-threonine derivative, a non-proteinogenic L-alpha-amino acid and an O-phosphoamino acid. It is a conjugate acid of an O-phosphonato-L-threonine(2-).
Synthesis of N-(4-bromobenzoyl)aminoethanethiol (A) and derivatization of phosphoserine and phosphothreonine residues (B).
Synthesis of N-(4-bromobenzoyl)aminoethanethiol (A) and derivatization of phosphoserine and phosphothreonine residues (B).
Zileuton
CAS number: 111406-87-2
Zileuton is a member of the class of 1-benzothiophenes that is 1-benzothiophene in which the hydrogen at position 2 is replaced by a 1-[carbamoyl(hydroxy)amino]ethyl group. A selective 5-lipoxygenase inhibitor, it inhibits the formation of leukotrienes LTB4, LTC4, LDT4, and LTE4. It is used for the management of chronic asthma. It has a role as an EC 1.13.11.34 (arachidonate 5-lipoxygenase) inhibitor, a non-steroidal anti-inflammatory drug, an anti-asthmatic drug, a leukotriene antagonist and a ferroptosis inhibitor. It is a member of ureas and a member of 1-benzothiophenes. It derives from a hydride of a 1-benzothiophene.
Pharmaceuticals containing the benzo[b]thiophene core structure: raloxifene, arzoxifene, zileuton, SB-271046, sertaconazole
Pharmaceuticals containing the benzo[b]thiophene core structure: raloxifene, arzoxifene, zileuton, SB-271046, sertaconazole
Naltrindole
CAS number: 111555-53-4
Naltrindole is a member of isoquinolines. Naltrindole (NTI), known as a delta opioid receptor antagonist, inhibited phorbol 12-myristate 13-acetate (PMA) induced superoxide (SO) release in polymorphonuclear leukocytes (PMNs).
Naltrindole, naltriben and selected analogs.
Naltrindole, naltriben and selected analogs.
Fischer synthesis of naltrindole and analogs from naltrexone.
Fischer synthesis of naltrindole and analogs from naltrexone.
Naltriben
CAS number: 111555-58-9
Naltriben is a morphinane alkaloid.
Naltrindole, naltriben and selected analogs.
Naltrindole, naltriben and selected analogs.