登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式(希尔记法):
C9H8
化学文摘社编号:
分子量:
116.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-393-6
Beilstein/REAXYS Number:
635873
MDL number:
Assay:
≥90%
Form:
liquid
SMILES string
C1C=Cc2ccccc12
InChI key
YBYIRNPNPLQARY-UHFFFAOYSA-N
InChI
1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
grade
technical grade
assay
≥90%
form
liquid
contains
50-100 ppm tert-butylcatechol as stabilizer
refractive index
n20/D 1.595 (lit.)
bp
181-182 °C (lit.)
mp
−5-−3 °C (lit.)
density
0.996 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
正在寻找类似产品? 访问 产品对比指南
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
136.4 °F - closed cup
flash_point_c
58 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Two-step synthesis of stable dioxadicarbaporphyrins from bis(3-indenyl)methane.
Timothy D Lash et al.
Angewandte Chemie (International ed. in English), 51(43), 10871-10875 (2012-09-25)
Lucas J Gursky et al.
Applied microbiology and biotechnology, 85(4), 995-1004 (2009-07-02)
The styAB genes from Pseudomonas putida CA-3, which encode styrene monooxygenase, were subjected to three rounds of in vitro evolution using error-prone polymerase chain reaction with a view to improving the rate of styrene oxide and indene oxide formation. Improvements
Regioselective synthesis of indenols by rhodium-catalyzed C-H activation and carbocyclization of aryl ketones and alkynes.
Krishnamoorthy Muralirajan et al.
Angewandte Chemie (International ed. in English), 50(18), 4169-4172 (2011-03-31)
Adam C Glass et al.
Organic letters, 10(21), 4855-4857 (2008-10-07)
A new methodology for the preparation of substituted naphthalenes starting from readily available indenones, organometal reagents, and trimethylsilyldiazomethane via a catalytic rearrangement process is described. Hindered biaryl naphthalenes, including triortho-substituted biaryls, can be accessed through our method. Our results are
Ermitas Alcalde et al.
Journal of medicinal chemistry, 52(3), 675-687 (2009-01-23)
Scaffold selection involving an indole-to-indene core change led to the discovery of a series of indenylsulfonamides that act as 5-HT6 serotonin receptor agonists. The variety of the targeted ligands and their synthetic complexity required multistep synthetic approaches. The novel indenylsulfonamides
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持
