535079
Bromomalonaldehyde
97%
Sinônimo(s):
Bromomalondialdehyde
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About This Item
Fórmula linear:
BrCH(CHO)2
Número CAS:
Peso molecular:
150.96
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
97%
pf
132-136 °C (lit.)
grupo funcional
aldehyde
bromo
cadeia de caracteres SMILES
[H]C(=O)C(Br)C([H])=O
InChI
1S/C3H3BrO2/c4-3(1-5)2-6/h1-3H
chave InChI
SURMYNZXHKLDFO-UHFFFAOYSA-N
Categorias relacionadas
Aplicação
Used in the formation of glyoxal-derived adducts from substituted guanines
Used to construct a 1,4-dihydroquinoline bearing a C-3 chiral sulfoxide group which functions as an annelated NADH model in the enantioselective reduction of methyl benzoylformate to methyl mandelate.
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Oral - Eye Dam. 1
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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Synlett, 441-441 (2005)
E C Taylor et al.
Investigational new drugs, 14(3), 281-285 (1996-01-01)
A new and extremely efficient synthesis of DDATHF from 4-vinylbenzoic acid and bromomalondialdehyde as precursors has been developed which proceeds in 48% overall yield.
Anne-Mari Ruohola et al.
Organic & biomolecular chemistry, 2(13), 1943-1950 (2004-07-01)
Reactions of 9-ethylguanine, 2'-deoxyguanosine and guanosine with bromomalondialdehyde in aqueous buffers over a wide pH-range were studied. The main products were isolated and characterized by (1)H and (13)C NMR and mass spectroscopy. The final products formed under acidic and basic
L Kronberg et al.
Chemical research in toxicology, 6(4), 495-499 (1993-07-01)
Mucochloric acid, a genotoxic compound formed during chlorine disinfection of drinking water, was reacted with adenosine and cytidine at pH 4.0, 90 degrees C. HPLC analyses with UV detection at 325 nm showed that one previously unidentified product peak was
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