109486-06-8 Usage
Derivative of isophthalaldehyde
It is a modified version of the parent compound isophthalaldehyde, with additional functional groups attached to its structure.
Benzene ring structure
The compound has a benzene ring as its core structure, which is a six-membered aromatic ring with alternating single and double bonds.
Hydroxyl and aldehyde functional groups
2,5-dihydroxyisophthalaldehyde has two hydroxyl (-OH) groups and one aldehyde (-CHO) functional group in its structure.
Position of functional groups
The hydroxyl groups are attached at positions 2 and 5 on the benzene ring, while the aldehyde group is also present in the structure.
Polymerization reactions
Due to its chemical structure, 2,5-dihydroxyisophthalaldehyde can undergo polymerization reactions, making it suitable for use in polymer chemistry and material science.
Potential applications in fluorescent sensors and optical materials
Researchers have studied 2,5-dihydroxyisophthalaldehyde for its possible use in developing sensors that emit light and optical materials with unique properties.
Building block for organic synthesis
The compound serves as an important building block in the synthesis of various organic compounds, making it of interest to researchers in organic chemistry and chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 109486-06-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,8 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109486-06:
(8*1)+(7*0)+(6*9)+(5*4)+(4*8)+(3*6)+(2*0)+(1*6)=138
138 % 10 = 8
So 109486-06-8 is a valid CAS Registry Number.
109486-06-8Relevant academic research and scientific papers
Petryk, Ma?gorzata,Janiak, Agnieszka,Kwit, Marcin
, p. 5825 - 5829 (2017)
Herein, an unusual tubular formation of a supramolecular organic framework by optically active macrocyclic calixsalen is shown via single crystal X-ray diffraction. The monomers are either bound by hydrogen bonds between OH groups in the lower rim of the macrocycle to form an hourglass structure or form a capsule with the calixsalens arranged in a head-to-head motif.
2,5- OR 2,6-DISUBSTITUTED HYDROQUINONE DERIVATIVES WITH AT LEAST ONE CARBOXY, SULFO OR AMIDO GROUP USEFUL AS MEDICAMENTS
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Paragraph 0160, (2021/09/16)
The invention provides hydroquinone derivatives of formula (I), processes of preparation, as well as pharmaceutical compositions and methods of treating and/or preventing e.g. autoimmune, immunological, rheumatology, vascular, ophthalmologic, fibrotic, me
