Structure

2-Bromo-3-hexylthiophene

CAS
69249-61-2
Catalog Number
ACM69249612-1
Category
Organic & Printed Electronics
Molecular Weight
247.20
Molecular Formula
C10H15BrS

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Specification

Description
2-Bromo-3-hexylthiophene is a monomeric precursor that forms bromo terminate polymers. It is synthesized by the bromination of hexylthiophene.
Synonyms
2-bromo-3-hexylthiophene;2-Bromo-3-nonylthiophene;Thiophene,2-broMo-3-hexyl-;2-Bromo-3-hexylthiophene 97%
IUPAC Name
2-bromo-3-hexylthiophene
SMILES
CCCCCCc1ccsc1Br
InChI
1S/C10H15BrS/c1-2-3-4-5-6-9-7-8-12-10(9)11/h7-8H,2-6H2,1H3
InChI Key
XQJNXCHDODCAJF-UHFFFAOYSA-N
Density
1.240 g/mL at 25 °C
Application
2-Bromo-3-hexylthiophene is majorly used in the formation of π-conjugated conductive polymers (CPs) for the fabrication of organic field effect transistors (OFETs) and organic photovoltaics (OPVs). The Grignard metathesis (GRIM) polymerization of 2-Bromo-3-hexylthiophene terminates a bromine and a proton at both ends to form conductive poly(3-hexylthiophene) (P3HT).
Storage
room temp
Assay
97%
Complexity
116
Covalently-Bonded Unit Count
1
Exact Mass
246.00778g/mol
Features And Benefits
1. High quality products
2. Fast delivery
3. Additional products can be ordered, please contact us for details
Formal Charge
0
H-Bond Acceptor
1
H-Bond Donor
0
Heavy Atom Count
12
MDL Number
MFCD09907959
Monoisotopic Mass
246.00778g/mol
NACRES
NA.23
Packaging
Packaging
1, 5 g in glass bottle
PubChem ID
329761448
Quality Level
100
Refractive Index
n20/D 1.529
Rotatable Bond Count
5
XLogP3
5.6
What is the product name of the compound with CAS number 69249-61-2?

The product name is 2-Bromo-3-hexylthiophene.

What category does 2-Bromo-3-hexylthiophene belong to?

It belongs to the Heterocyclic-1 Ring category.

How is 2-Bromo-3-hexylthiophene synthesized?

It is synthesized by the bromination of hexylthiophene.

What is the molecular weight of 2-Bromo-3-hexylthiophene?

Its molecular weight is 247.20.

What is the SMILES notation for 2-Bromo-3-hexylthiophene?

The SMILES notation is CCCCCCc1ccsc1Br.

What is the major application of 2-Bromo-3-hexylthiophene?

It is majorly used in the formation of π-conjugated conductive polymers for the fabrication of organic field effect transistors and organic photovoltaics.

How is the Grignard metathesis (GRIM) polymerization of 2-Bromo-3-hexylthiophene used?

It terminates a bromine and a proton at both ends to form conductive poly(3-hexylthiophene).

What purity level is guaranteed for this compound?

It has a minimum purity of 97%.

What are some features and benefits of 2-Bromo-3-hexylthiophene?

Some features and benefits include high quality products, fast delivery, and the option to order additional products.

How is 2-Bromo-3-hexylthiophene typically stored?

It is typically stored at room temperature.

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