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Merck
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文件

569364

Sigma-Aldrich

9,9-二辛基芴-2,7-二硼酸

96%

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About This Item

线性分子式:
(HO)2BC(C6H3C(C8H17)2C6H3B(OH)2
CAS号:
258865-48-4
分子量:
478.28
MDL號碼:
MFCD03701608
分類程式碼代碼:
12352103
PubChem物質ID:
24880497
NACRES:
NA.22

化驗

96%

mp

158-162 °C (lit.)

SMILES 字串

CCCCCCCCC1(CCCCCCCC)c2cc(ccc2-c3ccc(cc13)B(O)O)B(O)O

InChI

1S/C29H44B2O4/c1-3-5-7-9-11-13-19-29(20-14-12-10-8-6-4-2)27-21-23(30(32)33)15-17-25(27)26-18-16-24(31(34)35)22-28(26)29/h15-18,21-22,32-35H,3-14,19-20H2,1-2H3

InChI 密鑰

HURJMQMZDPOUOU-UHFFFAOYSA-N

相关类别

應用

9,9-Dioctylfluorene-2,7-diboronic acid can be used as a reactant to synthesize hyperbranched conjugated conductive copolymers by Pd-catalyzed Suzuki-Miyaura cross coupling (SMC) copolymerization reaction with different dibromoarenes.

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)

分析证书(COA)

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1-溴-4-苯乙炔 97%

Sigma-Aldrich

206512

1-溴-4-苯乙炔

Unexpected structural defects in a main-chain conjugated polymer synthesized through Suzuki-Miyaura cross coupling polymerization
Yuan Y, et al.
Polymer, 226, 123769-123769 (2021)
Synthesis of hyperbranched conjugated copolymers containing triphenylamine and fluorene or thiophene moieties
Grigoras M and Stafie L
High Performance Polymers, 21(3), 304-314 (2009)
Conjugated copolymers bearing 2, 7-dithienylphenanthrene-9, 10-dialkoxy units: highly soluble and stable deep-blue emissive materials
Baig N, et al.
New. J. Chem., 44(22), 9557-9564 (2020)
Zhiwei Chu et al.
Sensors (Basel, Switzerland), 18(5) (2018-05-16)
An aggregation-caused quenching (ACQ)-active polymer (PF), an aggregation-induced emission (AIE)-active polymer (PFTPE) and an aggregation-enhanced emission (AEE)-active polymer (PTTPE) were synthesized by tetraphenylethane (TPE), fluorene and thiophene moieties. Polyurethane (PU) foams modified by PF, PFTPE and PTTPE, namely PU-PF, PU-PFTPE

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