InChI
1S/C10H17NO/c1-2-8-6-11-4-3-9(8)5-10(11)7-12/h2,8-10,12H,1,3-7H2/t8-,9+,10+/m0/s1
SMILES string
OC[C@H]1CC2CCN1C[C@@H]2C=C
InChI key
GAFZBOMPQVRGKU-IVZWLZJFSA-N
assay
96%
optical activity
[α]20/D +189°, c = 1 in methanol
refractive index
n20/D 1.515 (lit.)
bp
267 °C (lit.)
density
1.073 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Application
在药物化学应用中很有价值的结构单元。该化合物的骨架和金鸡纳生物碱的骨架相同。可能的用途包括拆分剂、手性固定相以及不对称性合成中的手性配体。
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.0 °F - closed cup
flash_point_c
112.8 °C - closed cup
法规信息
新产品
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Ojima, I., ed.
Catalytic Asymmetric Synthesis (1993)
Resolution and adrenergic activities of the optical isomers of 4-[1-(1-naphthyl)ethyl]-1H-imidazole.
S S Hong et al.
Chirality, 4(7), 432-438 (1992-01-01)
Recently we synthesized a naphthalene analog of medetomidine, 4-[1-(1-naphthyl)ethyl]-1H-imidazole hydrochloride (1), and found it to be highly potent in adrenergic systems. The separation of optical isomers of this naphthalene analog was achieved by using the isomers of tartaric acid. The
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