124915
4-Formylbenzoic acid
97%
Sinonimo/i:
4-Carboxybenzaldehyde, Benzaldehyde-4-carboxylic acid, Terephthalaldehydic acid
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About This Item
Formula condensata:
HO2CC6H4CHO
Numero CAS:
Peso molecolare:
150.13
Beilstein:
471734
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
97%
Forma fisica
powder
Punto di fusione
247 °C (lit.)
Gruppo funzionale
aldehyde
carboxylic acid
Stringa SMILE
[H]C(=O)c1ccc(cc1)C(O)=O
InChI
1S/C8H6O3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5H,(H,10,11)
GOUHYARYYWKXHS-UHFFFAOYSA-N
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Descrizione generale
4-Formylbenzoic acid is an important intermediate in the synthesis of terepthalic acid. It reacts with barium carbonate to yield two-dimensional barium(II) coordination polymer.
Applicazioni
4-Formylbenzoic acid has been used as reagent during esterification of 2,2,6,6-tetramethyl-4-oxopiperidinyl-1-oxyl to yield 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl 4-formylbenzoate.
It can also be used as a reagent to synthesize acid functionalized mesoporous silica catalyst by the condensation of its aldehyde group with -NH2 of amine functionalized silica.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
Elena Sartori et al.
Journal of the American Chemical Society, 129(25), 7785-7792 (2007-06-05)
Interactions between reactive free radicals (r) with stable mononitroxyl radicals (N) and bisnitroxyl radicals (N-X-N) were studied by time-resolved electron paramagnetic resonance (TR-EPR). Reactive spin-polarized free radicals (r#), with non-Boltzmann population of spin states were produced by laser flash photolysis
The first two-dimensional barium coordination polymer based on neutral and deprotonated 4-formylbenzoic acid.
Deng ZP, et al.
Applied Organometallic Chemistry, 21(11), 978-982 (2007)
Topochemical studies. VIII. The crystal and molecular sturtures of two polymorphs of 4-formylbenzoic acid.
Haisa MASAO, et al.
Acta Crystallographica Section B, Structural Crystallography and Crystal Chemistry, 32(3), 857-860 (1976)
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This study focuses on the disassembly-behavior of self-immolative pro-fluorescent linkers under physiological conditions and through an enzyme-initiated domino reaction. The targeted linkers are based on para-aminobenzylalcohol (PABA) or hemithioaminal derivatives of para-carboxybenzaldehyde or glyoxilic acid. We found that a fine
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