112116-24-2

Basic information

• Product Name: 3,3’-(1,6-Hexanediyldioxy)bisbenzaldehyde
• Synonyms: 3,3’-(1,6-Hexanediyldioxy)bisbenzaldehyde;3,3’3,3'-(1,6-hexanediyldioxy) bisbenzaldeh
• CAS NO: 112116-24-2
• Molecular Formula: C₂₀H₂₂O₄
• Molecular Weight: 326.39
• Mol File: 112116-24-2.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 513.1±35.0 °C(Predicted)
• Appearance: /
• Density: 1.134±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 3,3’-(1,6-Hexanediyldioxy)bisbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3’-(1,6-Hexanediyldioxy)bisbenzaldehyde(112116-24-2)
• EPA Substance Registry System: 3,3’-(1,6-Hexanediyldioxy)bisbenzaldehyde(112116-24-2)

Safety Data

• Hazardous Substances Data: 112116-24-2(Hazardous Substances Data)

Upstream product

• 629-03-8 1 ,6-dibromohexane 
• 100-83-4 meta-hydroxybenzaldehyde 
• 4672-50-8 1,6-bis(p-toluenesulfonyloxy)hexane 
• 98-59-9 p-toluenesulfonyl chloride 
• 2163-00-0 1,6-dichlorohexane 

Downstream Products

• 862803-25-6 (CH₂)6(OC₆H₄CH(OH)CCH)2 
• 798577-28-3 (CH₂)6(OC₆H₄C(O)CCH)2 
• 1401456-79-8 N,N'-(5,5'-(3,3'-(hexane-1,6-diylbis(oxy))bis(3,1-phenylene))bis(4-acetyl-4,5-dihydro-1,3,4-thiadiazole-5,2-diyl))diacetamide 
• 1401456-66-3 2,2'-(3,3'-(hexane-1,6-diylbis(oxy))bis(3,1-phenylene))bis(methan-1-yl-1-ylidene)bis(hydrazinecarbothioamide) 

Relevant articles and documents

Synthesis, Antimicrobial Evaluations, and DNA Photo Cleavage Studies of New Bispyranopyrazoles

The bispyranopyrazoles (4a, 4b, 4c, 4d, 4e, 4f, 4g) were synthesized from the reactions of dibenzaldehydes (2a, 2b, 2c, 2d, 2e, 2f, 2g) with 3-methylpyrazole-5-one 3 and malononitrile by refluxing under alcoholic medium. The dibenzaldehydes were obtained from the O-alkylation of 3-hydroxybenzaldehyde with suitable 1,ω-dibromoalkanes under the alkaline conditions in the presence of dry EtOH/DMF. The structures of bisheterocyclics were determined from rigorous analysis of their spectral parameters (IR,1H-NMR,13C-NMR, and ESI-MS). The newly prepared compounds were screened for their antimicrobial activity against seven bacterial and five fungal strains. The DNA photo cleavage potential of these compounds was also evaluated by using agarose gel electrophoresis, and bispyranopyrazoles 4b, 4d and 4e exhibited significant level of DNA photocleavage activity.

Novel Bis(2-(5-((5-phenyl-1H-tetrazol-1-yl)methyl)-4H-1,2,4-triazol-3-yl)phenoxy)Alkanes: Synthesis and Characterization

In this study, 10 different substituted aromatic bis-benzaldehydes were synthesized by treating hydroxy benzaldehydes with various dihaloalkanes. Bis aldehydes 5a, 5b, 5c, 5d, 5e, 5f, 5g, 5h, 5i, 5j were treated with 2-(5-phenyl-1H-tetrazole-1-yl)acetohyd

New 1,3,4-bisthiadiazolines: Synthesis, characterization and antimicrobial evaluations

The bisthiadiazolines 4a-4g have been synthesized in good yields from the cyclization reactions of bisthiosemicarbazones 3a-3g with acetic anhydride. The condensation reaction of dibenzaldehydes 2a-2g with thiosemicarbazide in alcoholic medium provided 3a