3D-FF82399 - 3-4-fluorobenzyloxybenzaldehyde
4-Benzyloxybenzaldehyde
CAS:Formel:C14H12O2Reinheit:min. 98.0 %(GC)Farbe und Form:White to Light yellow powder to crystalMolekulargewicht:212.252-Benzyloxybenzaldehyde
CAS:Formel:C14H12O2Reinheit:>98.0%(GC)Farbe und Form:Colorless to Yellow clear liquidMolekulargewicht:212.253-Benzyloxybenzaldehyde
CAS:Formel:C14H12O2Reinheit:>98.0%(GC)Farbe und Form:White to Almost white powder to crystalMolekulargewicht:212.253-Benzyloxybenzaldehyde, 98%
CAS:3-Benzyloxybenzaldehyde is used as a pharmaceutical intermediate. It activates the adenyl cyclase. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar p
Formel:C14H12O2Reinheit:98%Farbe und Form:Powder, White to creamMolekulargewicht:212.253-Benzyloxybenzaldehyde
CAS:Formel:C14H12O2Reinheit:≥ 98.0%Farbe und Form:Yellow powderMolekulargewicht:212.253-Benzyloxybenzaldehyde-alpha-d1
CAS:Formel:C6H5CH2OC6H4CDOReinheit:98 atom % DFarbe und Form:White-Tan SolidMolekulargewicht:213.090012-Benzyloxybenzaldehyde
CAS:2-Benzyloxybenzaldehyde is an analog of benzaldehyde and can be used as a precursor for the synthesis of other molecules. It has been shown to inhibit the growth of HL-60 cells and xenograft tumor in mice. This compound also inhibits the production of cyclase, which is required to produce prostaglandin E2, a key regulator of inflammation in the body. This inhibition leads to an increase in mitochondrial membrane potential, leading to cell death by apoptosis. 2-Benzyloxybenzaldehyde also inhibits DNA binding activity and has been shown to induce fetal bovine serum levels and colony stimulating factor (CSF) levels in leukemic mice.Formel:C14H12O2Reinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:212.24 g/mol3-Benzyloxybenzaldehyde
CAS:3-Benzyloxybenzaldehyde (3BOBA) is a hydrochloride salt of 3-benzyloxybenzaldehyde. 3BOBA has shown anti-inflammatory activity in hl-60 cells and prostate cancer cells through inhibition of the activation of nuclear factor kappa B. This inhibition was found to be due to the apoptosis protein, survivin, which was downregulated by 3BOBA treatment. The analogs of 3BOBA are known as curcumin analogs, and have shown anticancer properties in clinical trials.Formel:C14H12O2Reinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:212.24 g/mol2-Methyl 4-benzyloxybenzaldehyde
CAS:Formel:C15H14O2Reinheit:96%Farbe und Form:SolidMolekulargewicht:226.2754-Benzyloxybenzaldehyde
CAS:Formel:C14H12O2Reinheit:97%Farbe und Form:Light yellow powderMolekulargewicht:212.2483-Benzyloxybenzaldehyde
CAS:Formel:C14H12O2Reinheit:98%Farbe und Form:Solid, ChunksMolekulargewicht:212.2484-Fluorobenzyloxybenzene
CAS:Formel:C13H11FOReinheit:98.0%Farbe und Form:SolidMolekulargewicht:202.2283-Fluorobenzyloxybenzene
CAS:Formel:C13H11FOReinheit:99.0%Farbe und Form:LiquidMolekulargewicht:202.2283-Benzyloxybenzaldehyde-α-d1
CAS:Kontrolliertes ProduktApplications 3-Benzyloxybenzaldehyde-alpha-d1 (CAS# 1219805-34-1) is a useful isotopically labeled research compound.
Formel:C14H11DO2Farbe und Form:NeatMolekulargewicht:213.254-Benzyloxybenzaldehyde
CAS:Kontrolliertes ProduktApplications 4-Benzyloxybenzaldehyde is a position isomer of the adenylyl cyclase activator 2-Benzyloxybenzaldehyde. 4-Benzyloxybenzaldehyde also has much less potent anticancer activity against HL-60 cells that its isomeric counterpart.
References Lin, C. et al.: Bioorg. Med. Chem., 13, 1537 (2005); Chang, C.-Y. et al.: Bioorg. Med. Chem. Lett., 11, 1971 (2001);Formel:C14H12O2Farbe und Form:NeatMolekulargewicht:212.244-Benzyloxybenzaldehyde
CAS:4-Benzyloxybenzaldehyde is a molecule with an aldehyde group and a benzyl alcohol group. It is the most active inhibitor of Candida glabrata among the compounds tested. 4-Benzyloxybenzaldehyde has been shown to inhibit Candida glabrata, Propionibacterium acnes, and Pseudomonas aeruginosa. This compound also inhibits hydrogen chloride production by Candida glabrata in vitro. 4-Benzyloxybenzaldehyde inhibits Candida glabrata by binding to the enzyme hydrogenase at the alpha-subunit's active site to prevent its function.
4-Benzyloxybenzaldehyde has been found to be more potent than benzoic acid in inhibiting candida growth, although less potent than gentamicin or erythromycin.Formel:C14H12O2Reinheit:Min. 95%Molekulargewicht:212.24 g/mol4-Benzyloxy-3,5-dimethylbenzaldehyde, 95%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formel:C16H16O2Reinheit:95%Farbe und Form:Clear yellow, LiquidMolekulargewicht:240.3








