124915
4-Formylbenzoic acid
97%
Sinônimo(s):
4-Carboxybenzaldehyde, Benzaldehyde-4-carboxylic acid, Terephthalaldehydic acid
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About This Item
Fórmula linear:
HO2CC6H4CHO
Número CAS:
Peso molecular:
150.13
Beilstein:
471734
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
97%
Formulário
powder
pf
247 °C (lit.)
grupo funcional
aldehyde
carboxylic acid
cadeia de caracteres SMILES
[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)
chave InChI
GOUHYARYYWKXHS-UHFFFAOYSA-N
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Descrição geral
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.
Aplicação
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.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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The first two-dimensional barium coordination polymer based on neutral and deprotonated 4-formylbenzoic acid.
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Topochemical studies. VIII. The crystal and molecular sturtures of two polymorphs of 4-formylbenzoic acid.
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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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