等级
purum
方案
≥97.0% (GC)
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.)
储存温度
2-8°C
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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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
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Peter Ongoma et al.
Dalton transactions (Cambridge, England : 2003), 41(35), 10724-10730 (2012-08-01)
The nucleophilic substitution reactions of complexes [Pt{4'-(2'''-CH(3)-phenyl)-2,2':6',2''-terpyridine}Cl]CF(3)SO(3), [CH(3)PhPtCl], [Pt{4'-(2'''-CH(3)-phenyl)-6-(3''-isoquinoyl)-2,2'bipyridine}Cl]SbF(6), [CH(3)PhisoqPtCl], [Pt{2-(2'-pyridyl)-1,10-phenanthroline}Cl]Cl, [pyPhenPtCl], and [Pt(terpyridine)Cl](+), [PtCl] with a series of nucleophiles: thiourea (TU), N,N-dimethylthiourea (DMTU), N,N,N,N-tetramethylthiourea (TMTU), I(-), Br(-), and SCN(-) were studied in 0.1 M LiCF(3)SO(3) in methanol (in the
Takashi Sugane et al.
Bioorganic & medicinal chemistry, 20(1), 34-41 (2011-12-20)
To identify novel glycine transporter 1(GlyT1) inhibitors with greater selectivity relative to GlyT2 and improved aqueous solubility, we synthesized a series of 4H-1,2,4-triazole derivatives with heteroaromatic rings at the 4-position and investigated their structure-activity relationships. Replacement of the 2-fluorophenyl group
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)
Hong Hou et al.
Chemical communications (Cambridge, England), 48(37), 4492-4494 (2012-03-30)
The unprecedented isoquinolinium zwitterionic salts with an unusual C-4 substitution pattern were efficiently prepared via the multicomponent reaction of in situ formed N-benzylisoquinolinium bromide with aromatic aldehydes and cyclic 1,3-dicarbonyl compounds.
Lian Chen et al.
Journal of medicinal chemistry, 55(12), 5965-5981 (2012-06-21)
Activation of the retinoid X receptor (RXR), which is involved in cell proliferation, differentiation, and apoptosis, is a strategy for cancer chemotherapy and chemoprevention, and 3-amino-6-(3'-aminopropyl)-5H-indeno[1,2-c]isoquinoline-5,11-(6H)dione (AM6-36) (3) is among the few RXR ligands known. The presently reported studies of
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