166391
1-Formylpyrrolidine
97%
Sinônimo(s):
Pyrrolidine-1-carboxaldehyde
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25 G
R$ 1.085,00
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25 G
R$ 1.085,00
About This Item
Fórmula empírica (Notação de Hill):
C5H9NO
Número CAS:
Peso molecular:
99.13
Beilstein:
106540
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
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Nível de qualidade
Ensaio
97%
Formulário
liquid
índice de refração
n20/D 1.479 (lit.)
p.e.
92-94 °C/15 mmHg (lit.)
densidade
1.04 g/mL at 25 °C (lit.)
cadeia de caracteres SMILES
[H]C(=O)N1CCCC1
InChI
1S/C5H9NO/c7-5-6-3-1-2-4-6/h5H,1-4H2
chave InChI
AGRIQBHIKABLPJ-UHFFFAOYSA-N
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Descrição geral
1-Formylpyrrolidine is the monomer constituent of gas clathrate inhibitor[1].
Aplicação
1-Formylpyrrolidine was used in the synthesis of 1-oxa-3,4-dimethyl-5-(1-pyrrolldino)-2,2-di(tert-butyl)silacyclopentane and 1-oxa-4-isopropyl-5-(1-pyrrolidino)-2,2-di(tert-butyl)silacyclopentane[2].
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
203.0 °F - closed cup
Ponto de fulgor (°C)
95 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves
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Journal of medicinal chemistry, 37(13), 2071-2078 (1994-06-24)
New compounds were synthesized by structural modification of 1-[1-(4-phenylbutanoyl)-L-prolyl]-pyrrolidine (SUAM-1221, 1) or 1-[1-(benzyloxycarbonyl)-L-proly]prolinal (Z-Pro-prolinal,2) and were tested for in vitro inhibitory activities against purified prolyl endopeptidase (PEP) from canine brain. In a series of compounds which lack a formyl or
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Homochiral E and Z isomers of N-methylprolinal O-isopropyloxime and (1-methyl-2-pyrrolidinyl)methoxyimines were synthesized as candidate bioisosteres of nicotine and its isoxazolic analogue ABT 418. Two of them, namely (S)-2-isopropylideneaminooxymethyl- and (Z)-(S)-2-ethylideneaminooxymethyl-1-methylpyrrolidine, proved to bind at alpha4beta2 nicotinic acetylcholine receptor with submicromolar
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Journal of enzyme inhibition, 3(3), 163-178 (1990-01-01)
Several prolinal derivatives were synthesized and examined for their inhibitory activity on post-proline cleaving enzymes from Flavobacterium meningosepticum and bovine brain and their possible properties as nootropic agents. Almost all the compounds tested inhibited the activity of both enzymes at
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