714844
4-(Dimethylamino)pyridine solution
0.5 M in THF
Sinônimo(s):
DMAP solution
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About This Item
Fórmula empírica (Notação de Hill):
C7H10N2
Número CAS:
Peso molecular:
122.17
Beilstein:
3539759
Número MDL:
Código UNSPSC:
12352005
ID de substância PubChem:
Produtos recomendados
forma
liquid
concentração
0.5 M in THF
índice de refração
n20/D 1.417
densidade
0.884 g/mL at 25 °C
cadeia de caracteres SMILES
CN(C)c1ccncc1
InChI
1S/C7H10N2/c1-9(2)7-3-5-8-6-4-7/h3-6H,1-2H3
chave InChI
VHYFNPMBLIVWCW-UHFFFAOYSA-N
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A generic LC-MS/MS method was developed for the analysis of potentially genotoxic alkyl halides. A broad selection of alkyl halides were derivatized using 4-dimethylaminopyridine in acetonitrile. The reaction conditions for derivatization, i.e., solvent, reaction time, temperature and concentration of alkyl
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To maximize therapeutic effects, targeted delivery of nucleic acids (e.g., DNA and RNA) in their appropriate intracellular targets is highly desirable. In this study, primary amines of a model polymeric nonviral carrier, polyethylenimine (PEI), at two molecular weights (0.8 and
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Catalysts hold promise as tools for chemical protein modification. However, the application of catalysts or catalyst-mediated reactions to proteins has only recently begun to be addressed, mainly in in vitro systems. By radically improving the affinity-guided DMAP (4-dimethylaminopyridine) (AGD) catalysts
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An effective method for grafting L-lactide (LA) from unmodified cellulose by ring-opening polymerization (ROP) in homogeneous mild conditions is presented. By using 4-dimethylaminopyridine (DMAP) as an organic catalyst, cellulose-graft-poly(L-lactide) (cellulose-g-PLLA) copolymers with a molar substitution (MS(PLLA)) of PLLA in a
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