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576700

2,2′-Bithiophene-5-carboxaldehyde

Name: 2,2′-Bithiophene-5-carboxaldehyde
Brand: ALDRICH

98%

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About This Item

Empirical Formula (Hill Notation):

C₉H₆OS₂

CAS Number:

3779-27-9

Molecular Weight:

194.27

NACRES:

NA.22

PubChem Substance ID:

24880877

UNSPSC Code:

12352100

MDL number:

MFCD00052294

Assay:

98%

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Properties

assay

98%

mp

55-58 °C (lit.)

functional group

aldehyde

SMILES string

[H]C(=O)c1ccc(s1)-c2cccs2

InChI

1S/C9H6OS2/c10-6-7-3-4-9(12-7)8-2-1-5-11-8/h1-6H

InChI key

FYBWRAXKYXTOQC-UHFFFAOYSA-N

Description

Application

2,2′-Bithiophene-5-carboxaldehyde may be used in the synthesis of the following:

boron dipyrromethene(BODIPY)oligothiophenes via a multi-step reaction process
(2,2′-bithiophene-5-carbaldehyde)-4-nitrophenylhydrazone(BT-NPH) via reaction with 4-nitrophenylhydrazine
bithiophene fulleropyrrolidine obtained via refluxing with sarcosine and fullerene
azomethine phthalic diimides by heating with N,N-bis(4-amino-2,3,5,6-tetramethylphenyl)naphthalene-1,4,5,8-dicarboximide (DANDI)

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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"Optical nonlinearities and molecular conformations in thiophene-based hydrazone crystals"

Kwon P-O, et al.

The Journal of Physical Chemistry C, 113(34), 15405-15411 (2009)

"The effect of thiophene substituents of fulleropyrrolidine acceptors on the performance of inverted organic solar cells"

Kaunisto.MK, et al.

Synthetic Metals, 195, 193-200 (2014)

"New low band gap compounds comprised of naphthalene diimide and imine units"

Schab-Balcerzak E, et al.

Synthetic Metals, 162(05), 543- 553 (2012)

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Global Trade Item Number

SKU	GTIN
576700-1G	04061826279991
576700-5G	04061832628776