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459968

1,2,3,4-四苯基-1,3-环戊二烯

Name: 1,2,3,4-四苯基-1,3-环戊二烯
Brand: ALDRICH

95%

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关于此项目

经验公式（希尔记法）:

C₂₉H₂₂

化学文摘社编号:

15570-45-3

分子量:

370.48

NACRES:

NA.22

PubChem Substance ID:

24869624

UNSPSC Code:

12352100

EC Number:

239-619-8

MDL number:

MFCD00001355

Assay:

95%

Form:

solid

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属性

Quality Level

100

assay

95%

form

solid

mp

180-182 °C (lit.)

functional group

phenyl

SMILES string

C1C(c2ccccc2)=C(c3ccccc3)C(c4ccccc4)=C1c5ccccc5

InChI

1S/C29H22/c1-5-13-22(14-6-1)26-21-27(23-15-7-2-8-16-23)29(25-19-11-4-12-20-25)28(26)24-17-9-3-10-18-24/h1-20H,21H2

InChI key

JCXLYAWYOTYWKM-UHFFFAOYSA-N

说明

General description

1,2,3,4-Tetraphenyl-1,3-cyclopentadiene is formed as one of the condensation products during the reactions of diphenylacetylene with methylchromium systems.

Application

1,2,3,4-Tetraphenyl-1,3-cyclopentadiene (TPCP) may be employed for the fabrication of triple-layer blue-emitting device.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

SHBJ9969

SHBF3956V

10813EQ

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Formation of 1, 3, 4, 5-tetraphenyl-2, 6, 7-trioxabicyclo [3.2. 1] oct-3-ene from the ozonolysis of 1, 2, 3, 4-tetraphenyl-1, 3-cyclopentadiene. First [3+ 4] addition of a carbonyl oxide moiety to an. alpha.,. beta.-unsaturated carbonyl group.

Mori M, et al.

Journal of the American Chemical Society, 109(14), 4407-4408 (1987)

Effect of electric field strength on the electroluminescence spectra of a blue-emitting device.

Cao H, et al.

Synthetic Metals, 96(3), 191-194 (1998)

Cyclization of diphenylacetylene on methylchromium s-complexes II. Cyclic and linear condensations.

Michman M and Zeiss HH.

Journal of Organometallic Chemistry, 25(1), 161-166 (1970)

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货号	GTIN
459968-1G	04061826663738