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D204803

Sigma-Aldrich

二苯基乙炔

98%

别名:

二苯乙炔

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About This Item

线性分子式:
C6H5C≡CC6H5
CAS号:
501-65-5
分子量:
178.23
Beilstein:
606478
EC號碼:
207-926-6
MDL號碼:
MFCD00004786
分類程式碼代碼:
12352100
PubChem物質ID:
24893607
NACRES:
NA.22

品質等級

100

化驗

98%

形狀

crystals

bp

170 °C/19 mmHg (lit.)

mp

59-61 °C (lit.)

密度

0.99 g/mL at 25 °C (lit.)

SMILES 字串

c1ccc(cc1)C#Cc2ccccc2

InChI

1S/C14H10/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H

InChI 密鑰

JRXXLCKWQFKACW-UHFFFAOYSA-N

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相关类别

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SDBB0672
STBL4535
STBJ4099
STBG3433V
STBF1960V

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Anion-dependent switching: dynamically controlling the conformation of hydrogen-bonded diphenylacetylenes.
Ian M Jones et al.
Angewandte Chemie (International ed. in English), 50(20), 4597-4600 (2011-04-16)
Dai Nishimura et al.
The Journal of organic chemistry, 73(7), 2496-2502 (2008-03-14)
Novel [2]rotaxanes bearing alpha-cyclodextrin (alpha-CD) derivatives and a diphenylacetylene axis molecule with trinitrobenzene as a bulky stopper have been prepared to investigate the relative rotary movement of a ring relative to an axis molecule and that of an axis molecule
Rajesh Chandra et al.
Journal of medicinal chemistry, 50(10), 2415-2423 (2007-04-24)
A series of 18F fluoropegylated diphenylacetylenes as probes for binding to Abeta plaques were successfully prepared. These relatively rigid acetylenes, 12a, 12b, 14a, and 14b, displayed high binding affinities in postmortem AD brain homogenates (Ki ranging from 1.2 to 2.9
Wenjing Hong et al.
Journal of the American Chemical Society, 134(4), 2292-2304 (2011-12-20)
Employing a scanning tunneling microscopy based beak junction technique and mechanically controlled break junction experiments, we investigated tolane (diphenylacetylene)-type single molecular junctions having four different anchoring groups (SH, pyridyl (PY), NH(2), and CN) at a solid/liquid interface. The combination of
Jim C Spain et al.
Applied and environmental microbiology, 69(7), 4037-4042 (2003-07-04)
Several strategies for using enzymes to catalyze reactions leading to the synthesis of relatively simple substituted picolinic acids have been described. The goal of the work described here was to synthesize a more complex molecule, 6-phenylacetylene picolinic acid [6-(2-phenylethynyl)pyridine-2-carboxylic acid]
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