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Merck
CN

757241

9-(9-Heptadecanyl)-9H-carbazole-2,7-diboronic acid bis(pinacol) ester

97%

Synonym(s):

9-(1-Octylnonyl)-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole

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About This Item

Empirical Formula (Hill Notation):
C41H65B2NO4
CAS Number:
958261-51-3
Molecular Weight:
657.58
NACRES:
NA.23
PubChem Substance ID:
329766660
UNSPSC Code:
12352103
MDL number:
MFCD16621134

Key Documents

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InChI

1S/C41H65B2NO4/c1-11-13-15-17-19-21-23-33(24-22-20-18-16-14-12-2)44-36-29-31(42-45-38(3,4)39(5,6)46-42)25-27-34(36)35-28-26-32(30-37(35)44)43-47-40(7,8)41(9,10)48-43/h25-30,33H,11-24H2,1-10H3

SMILES string

CCCCCCCCC(CCCCCCCC)n1c2cc(ccc2c3ccc(cc13)B4OC(C)(C)C(C)(C)O4)B5OC(C)(C)C(C)(C)O5

InChI key

XMKFCPVHTTWWCK-UHFFFAOYSA-N

assay

97%

form

powder

Application

9-(9-Heptadecanyl)-9H-carbazole-2,7-diboronic acid bis(pinacol) ester can be used in the synthesis of organic semiconducting polymers for optoelectronic applications such as organic photovoltaics.
This material is used in the formation of low band gap semiconducting materials for low cost plastic solar cells

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBK1978

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Incorporation of different conjugated linkers into low band gap polymers based on 5, 6-Bis (octyloxy)-2, 1, 3 benzooxadiazole for tuning optoelectronic properties
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Journal of Polymer Science Part A: Polymer Chemistry, 54(16), 2459-2467 (2016)

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