等级
technical grade
方案
90-92%
表单
solid
折射率
n20/D 1.623 (lit.)
沸点
242-243 °C (lit.)
mp
26-28 °C (lit.)
密度
1.099 g/mL at 25 °C (lit.)
SMILES字符串
c1ccc2cnccc2c1
InChI
1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H
InChI key
AWJUIBRHMBBTKR-UHFFFAOYSA-N
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一般描述
The intensity of fluorescence peak of isoquinoline increases with increasing pressure in polymethylmethacrylate and in polyisobutylene polymeric media.
应用
Isoquinoline (isq) has been used:
- in the preparation of cis-[(dcbH2)2Ru(isq)2](ClO4)2 [dcbH2 = 4,4′-(CO2H)2-2,2′-bipyridine]
- to investigate the toxicity of three two-ring and five three-ring azaarenes to the green alga Scenedesmus acuminatus and its relationship with molecular structure
警示用语：
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
闪点(°F)
215.6 °F - closed cup
闪点(°C)
102 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Sensitization of n-type TiO2 electrode by a novel isoquinoline ruthenium (II) polypyridyl complex.
Garcia CG, et al.
Journal of the Brazilian Chemical Society, 9(1), 13-15 (1998)
Property-toxicity relationships of azaarenes to the green alga Scenedesmus acuminatus.
Vlaardingen V, et al.
Environmental Toxicology and Chemistry / Setac, 15(11), 2035-2042 (1996)
High pressure studies of isoquinoline luminescence in polymeric media.
Rollinson AM, et al.
Chemical Physics Letters, 59(3), 559-561 (1978)
Viktoras Dryza et al.
The journal of physical chemistry. A, 116(17), 4323-4329 (2012-04-14)
Electronic spectra of the gas-phase isoquinoline(+)-Ar and quinoline(+)-Ar complexes are recorded using photodissociation spectroscopy by monitoring the Ar loss channel. The D(3)←D(0) and D(4)←D(0) band origins for isoquinoline(+)-Ar are observed at 15245 ± 15 cm(-1) and 21960 ± 15 cm(-1)
Jeremy Shonberg et al.
Journal of medicinal chemistry, 56(22), 9199-9221 (2013-10-22)
Biased agonism offers an opportunity for the medicinal chemist to discover pathway-selective ligands for GPCRs. A number of studies have suggested that biased agonism at the dopamine D2 receptor (D2R) may be advantageous for the treatment of neuropsychiatric disorders, including
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