Results 221 to 230 of about 49,863 (262)

Total Electrosynthesis of N, N-Dimethylformamide From CO₂ and NO₃. [PDF]

Adv Sci (Weinh)
Yan S, Chen S, McKee M, Terry A, Weisbarth R, Kornienko N.   +5 more
europepmc   +1 more source

Discovery of CRBN-recruiting PROTAC degraders of the METTL3-METTL14 complex. [PDF]

Med Chem Res
Smith AR, Nar R, Li Y, Gour A, Sharma A, Qian Z, Zheng G, Wu Z.   +7 more
europepmc   +1 more source

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Methylamine

2022
The German Commission for the Investigation of Health Hazards of Chemical Compounds in the Work Area has re-evaluated methylamine [74-89-574-89-5]. The critical effect is irritation of the nasal airways as observed in a 2-week study in rats with a NOAEC of 75 ml/m3.
Hartwig, Andrea, MAK Commission
openaire   +1 more source

Methylamine in human urine

Clinica Chimica Acta, 2001
Methylamine is the simplest aliphatic amine found in human urine. In the body it is thought to play a significant part in central nervous system disturbances observed during renal and hepatic disease and also has a role in general toxicity caused by oxidative stress.
S C, Mitchell, A Q, Zhang
openaire   +2 more sources

Dihydrobis(methylamine)borate triiodide

Acta Crystallographica Section C Crystal Structure Communications, 2006
Both cation and anion in the title compound, C2H12BN2+.I3-, lie on a crystallographic mirror plane and are bound in the lattice by N-H...I- hydrogen bonds, forming layers. Methyl-H-borane-H dihydride [-C-H(delta+)...(delta-)H-B-] interactions between molecules crosslink adjacent layers, giving ;sandwich' stacking along the a axis.
Graeme J, Gainsford, Tim, Kemmitt
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Enzymology of Methylamine Dehydrogenase

1996
Methylamine dehydrogenase (MADH) belongs to the class of quinoprotein enzymes because it has tryptophyl tryptophanquinone (TTQ) as cofactor. In most cases, it is clear that the small blue copper protein, amicyanin, functions as natural electron acceptor.
Gorren, A.F.C., van der Palen, C.J.N.M., van Spanning, Rob, Duine, J.A.   +3 more
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Microwave Spectrum of Methylamine (I)

Journal of the Physical Society of Japan, 1953
Microwave spectrum of methylamine molecule has been studied in the frequency range between 7 and 30 kMc/sec. More than two hundred lines and their Stark effects have been measured. These lines are divided into three kinds: (1) Δ J =0, Δ K =±1, (2) Δ J =±1, \(\varDelta K{=}{\mp}1\), and (3) Δ J =0, Δ K =0.
Koichi Shimoda, Tetsuji Nishikawa
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Methylamination of some 3-nitro-1,5-naphthyridines with liquid methylamine/potassium permanganate

Journal of Heterocyclic Chemistry, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Maria Grzegozek, Barbara Szpakiewicz
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