跳转至内容
Merck
CN

58740

异喹啉

purum, ≥97.0% (GC)

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式(希尔记法):
C9H7N
化学文摘社编号:
分子量:
129.16
EC Number:
204-341-8
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
107549
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


grade

purum

assay

≥97.0% (GC)

refractive index

n20/D 1.623 (lit.)

bp

242-243 °C (lit.)

mp

26-28 °C (lit.)

density

1.099 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

c1ccc2cnccc2c1

InChI

1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H

InChI key

AWJUIBRHMBBTKR-UHFFFAOYSA-N



Still not finding the right product?

Explore all of our products under 异喹啉


pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

法规信息

新产品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如需帮助,请联系 客户支持

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库



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)
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
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