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化驗
99%
形狀
solid
mp
74-76 °C (lit.)
官能基
amine
hydroxyl
phenyl
SMILES 字串
CNCC(O)c1ccccc1
InChI
1S/C9H13NO/c1-10-7-9(11)8-5-3-2-4-6-8/h2-6,9-11H,7H2,1H3
InChI 密鑰
ZCTYHONEGJTYQV-UHFFFAOYSA-N
一般說明
作为可能的底物,用于涉及苯乙醇胺-N-甲基转移酶的研究。
應用
α-(Methylaminomethyl)benzyl alcohol was used in the synthesis of 1,4-disubstituted-2,3,4,5-tetrahydro-1H-3-benzazepines. It was also used as internal standard during determination of pseudoephedrine and phenylpropanolamine urine concentrations by HPLC.
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Progress in neuro-psychopharmacology & biological psychiatry, 8(3), 385-395 (1984-01-01)
The radiotracers, C-14-N-methylphenylethylamine (MPEA) and N-methylphenylethanolamine (MPEOA) both rapidly entered mouse brain after their intravenous injection and were metabolized by brain monoamine oxidase (MAO) to C-14-methylamine and corresponding aldehydes. The labelled metabolite was trapped in the brain. Measurement of radioactivity
British journal of clinical pharmacology, 57(1), 62-67 (2003-12-18)
To study the elimination of ephedrines with reference to the International Olympic Committee (IOC) doping control cut-off levels, following multiple dosing of over-the-counter decongestant preparations. A double-blind study was performed in which 16 healthy male volunteers were administered either pseudoephedrine
The vasoactive potential of halostachine, an alkaloid of tall fescue (Festuca arundinaceae, Schreb) in cattle.
Veterinary and human toxicology, 25(6), 408-411 (1983-12-01)
The Journal of pharmacology and experimental therapeutics, 217(2), 379-385 (1981-05-01)
Single i.v. doses of the endogenous trace amine phenylethanolamine (PEOH) and its N-methyl homolog (NMPEOH) were administered to separate groups of five dogs. The dose- and time-related effects of these compounds were measured on pupillary diameter, heart rate and body
Organic letters, 2(25), 4099-4102 (2000-12-12)
[structure] Two general routes to 1,4-disubstituted-2,3,4, 5-tetrahydro-1H-3-benzazepines are described. Both routes utilize an appropriately functionalized phenethylamino alcohol as the penultimate intermediate: the first route makes use of the reductive amination of a benzyl alkyl ketone with alpha-(aminomethyl)benzyl alcohol, while the
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