324751-00-0

Basic information

• Product Name: 3-(Quinolin-2-yl)benzaldehyde
• Synonyms: 3,3'-(3,5-Pyridinediyl)bisbenzaldehyde;3,3'-(4,6-Pyrimidinediyl)bisbenzaldehyde;9,10-Bis(3-formylphenyl)anthracene;3-(Quinolin-2-yl)benzaldehyde;3,3'-(2,6-Pyrazinediyl)bisbenzaldehyde;3,3'-(2,6-Pyridinediyl)bisbenzaldehyde
• CAS NO: 324751-00-0
• Molecular Formula: C₂₈H₁₈O₂
• Molecular Weight: 386.44
• Mol File: 324751-00-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(Quinolin-2-yl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Quinolin-2-yl)benzaldehyde(324751-00-0)
• EPA Substance Registry System: 3-(Quinolin-2-yl)benzaldehyde(324751-00-0)

Safety Data

• Hazardous Substances Data: 324751-00-0(Hazardous Substances Data)

Upstream product

• 523-27-3 9,10-Dibromoanthracene 
• 87199-16-4 3-Formylphenylboronic acid 

Downstream Products

• 324751-04-4 9,10-bis[3-(4,4,5,5-tetramethyl-1,3-dihydroxyimidazolidin-2-yl)phenyl]anthracene 

Relevant articles and documents

Luminescence Ratiometric Nanothermometry Regulated by Tailoring Annihilators of Triplet–Triplet Annihilation Upconversion Nanomicelles

Triplet–triplet annihilation (TTA) upconversion is a special non-linear photophysical process that converts low-energy photons into high-energy photons based on sensitizer/annihilator pairs. Here, we constructed a novel luminescence ratiometric nanothermo

π-topology and spin alignment utilizing the excited molecular field: Observation of the excited high-spin quartet (S = 3/2) and quintet (S = 2) states on purely organic π-conjugated spin systems

As a model system for the photoinduced/photoswitched spin alignment in a purely organic π-conjugated spin system, 9-[4-(4,4,5,5-tetramethyl-1-yloxyimidazolin-2-yl)phenyl]-anthracene (1a), 9-[3-(4,4,5,5-tetramethyl-1-yloxyimidazolin-2-yl)phenyl]anthracene