Home Other Building Blocks 2-Bromo-3-hexylthiophene

2-Bromo-3-hexylthiophene

CAS No.:
69249-61-2
Catalog Number:
AG003GMW
Molecular Formula:
C10H15BrS
Molecular Weight:
247.1951
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$12
- +
5g
97%
In Stock USA
United States
$44
- +
10g
97%
In Stock USA
United States
$75
- +
25g
97%
In Stock USA
United States
$125
- +
100g
97%
In Stock USA
United States
$375
- +
Product Description
Catalog Number:
AG003GMW
Chemical Name:
2-Bromo-3-hexylthiophene
CAS Number:
69249-61-2
Molecular Formula:
C10H15BrS
Molecular Weight:
247.1951
MDL Number:
MFCD09907959
IUPAC Name:
2-bromo-3-hexylthiophene
InChI:
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
SMILES:
CCCCCCc1ccsc1Br
Properties
Complexity:
116  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
246.008g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
247.194g/mol
Monoisotopic Mass:
246.008g/mol
Rotatable Bond Count:
5  
Topological Polar Surface Area:
28.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5.6  
Literature
Title Journal
Synthesis of end-capped regioregular poly(3-hexylthiophene)s via direct arylation. Macromolecular rapid communications 20120726
Nickel(II) α-diimine catalyst for Grignard metathesis (GRIM) polymerization. Macromolecular rapid communications 20111101
Synthesis of well-defined head-to-tail-type oligothiophenes by regioselective deprotonation of 3-substituted thiophenes and nickel-catalyzed cross-coupling reaction. Journal of the American Chemical Society 20111026
Palladium-catalyzed dehydrohalogenative polycondensation of 2-bromo-3-hexylthiophene: an efficient approach to head-to-tail poly(3-hexylthiophene). Journal of the American Chemical Society 20100825
A case report of acute dermatitis that developed during an experiment examining the bromination of 3-hexylthiophene. Journal of occupational medicine and toxicology (London, England) 20100101
Properties