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Key Documents

168769

Sigma-Aldrich

98%

同義詞:

Indonaphthene

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About This Item

經驗公式(希爾表示法):
C9H8
CAS號碼:
分子量::
116.16
Beilstein:
635873
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
eCl@ss:
39011614
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

liquid

折射率

n20/D 1.595 (lit.)

bp

181-182 °C (lit.)

mp

−5-−3 °C (lit.)

溶解度

organic solvents: miscible
water: insoluble

密度

0.996 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

C1C=Cc2ccccc12

InChI

1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2

InChI 密鑰

YBYIRNPNPLQARY-UHFFFAOYSA-N

尋找類似的產品? 前往 產品比較指南

一般說明

通过 恶臭假单胞菌 红球菌 将茚氧化为 顺式 -和 反式 -茚满二醇及相关代谢产物的混合物。

應用

茚用于合成新的 C 60 衍生物茚-C 60 双加合物 。在 CH 2 Cl 2 中,用甲基异丙醚/TiCl 4 引发控制阳离子聚合制备聚茚。

象形圖

FlameHealth hazard

訊號詞

Danger

危險聲明

危險分類

Asp. Tox. 1 - Flam. Liq. 3

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

136.4 °F - closed cup

閃點(°C)

58 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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High glass transition temperature polyolefins obtained by the catalytic hydrogenation of polyindene.
Hahn SF and Hillmyer MA.
Macromolecules, 36(1), 71-76 (2003)
B C Buckland et al.
Metabolic engineering, 1(1), 63-74 (2000-08-10)
Indene is oxidized to mixtures of cis- and trans-indandiols and related metabolites by Pseudomonas putida and Rhodococcus sp. isolates. Indene metabolism is consistent with monooxygenase and dioxygenase activity. P. putida resolves enantiomeric mixtures of cis-1,2-indandiol by further selective oxidation of
Youjun He et al.
Journal of the American Chemical Society, 132(4), 1377-1382 (2010-01-09)
Polymer solar cells (PSCs) are commonly composed of a blend film of a conjugated polymer donor and a soluble C(60) derivative acceptor sandwiched between an ITO anode and a low-workfunction metal cathode. Poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C-61-butyric acid methyl ester (PCBM)
Ram Shankar Upadhayaya et al.
Organic & biomolecular chemistry, 8(24), 5661-5673 (2010-10-12)
Prompted by our discovery of a new class of conformationally-locked indeno[2,1-c]quinolines as anti-mycobacterials, compounds 2a and 3a (Fig. 1; MIC < 0.39 μg mL(-1) and 0.78 μg mL(-1), respectively)(14) with a freely rotating C2-imidazolo substituent, we herein describe the synthesis
Song Tu et al.
Journal of agricultural and food chemistry, 56(13), 5247-5253 (2008-06-13)
Nineteen novel indene-substituted oxime ether strobilurins, which used an indene group to stabilize the ( E)-styryl group in SYP-Z071 (an unsaturated oxime strobilurin fungicide under development by the Shenyang Research Institute of Chemical Industry), were designed and synthesized. The biological

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