质量水平
检测方案
99%
旋光性
[α]22/D −4°, c = 20 in H2O
mp
227-229 °C (lit.)
SMILES字符串
Cl.Cl.C[C@H](N)CN
InChI
1S/C3H10N2.2ClH/c1-3(5)2-4;;/h3H,2,4-5H2,1H3;2*1H/t3-;;/m0../s1
InChI key
AEIAMRMQKCPGJR-QTNFYWBSSA-N
应用
(S)-(-)-1,2-Diaminopropane dihydrochloride may be used in the preparation of following chiral imidazoline derivatives, which show moderate α-adrenergic blocking activity:
- (S)-(-)-4-methyl-2-(1-naphthylmethyl)imidazoline hydrochloride
- (S)-(-)-2-benzyl-4-methylimidazoline picrate
- (S )-(-)-2-[(2,6-dichlorophenyl)imino]-4-methylimidazolidine hydrochloride
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Stereochemical studies of adrenergic drugs. Optically active derivatives of imidazolines.
Journal of Medicinal Chemistry, 19(12), 1382-1384 (1976)
Optically active derivatives of imidazolines: a-Adrenergic blocking properties.
Journal of Medicinal Chemistry, 23(11), 1232-1235 (1980)
Bioorganic & medicinal chemistry letters, 21(22), 6909-6915 (2011-10-07)
The synthesis, evaluation, and structure-activity relationships of a set of related constrained diaminopropane inhibitors of BACE-1 are described. The full in vivo profile of an optimized inhibitor in both normal and P-gp deficient mice is compared with data generated in
The Biochemical journal, 280 ( Pt 3), 825-827 (1991-12-15)
1. L-Ornithine transport by plasma-membrane vesicles isolated from Ehrlich cells is Na(+)-independent and shows a saturable and a diffusional component. 2. Putrescine, histamine, 5-hydroxytryptamine and 2,3-diaminopropane at 55 microM concentration significantly inhibit 0.5 mM-L-ornithine transport at least for the first
Chiral cyanide-bridged Mn(II)Mn(III) ferrimagnets, [Mn(II)(HL)(H2O)][Mn(III)(CN)6].2H2O (L = S- or R-1,2-diaminopropane): syntheses, structures, and magnetic behaviors.
Journal of the American Chemical Society, 129(2), 248-249 (2007-01-11)
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