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15155-41-6 | 2,1,3-Benzothiadiazole, 4,7-dibromo-
CAS No: 15155-41-6 Catalog No: AG001NF6 MDL No:MFCD00658844
Product Description
Catalog Number:
AG001NF6
Chemical Name:
2,1,3-Benzothiadiazole, 4,7-dibromo-
CAS Number:
15155-41-6
Molecular Formula:
C6H2Br2N2S
Molecular Weight:
293.9665
MDL Number:
MFCD00658844
IUPAC Name:
4,7-dibromo-2,1,3-benzothiadiazole
InChI:
InChI=1S/C6H2Br2N2S/c7-3-1-2-4(8)6-5(3)9-11-10-6/h1-2H
InChI Key:
FEOWHLLJXAECMU-UHFFFAOYSA-N
SMILES:
Brc1ccc(c2c1nsn2)Br
Properties
Complexity:
142
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
293.828g/mol
Formal Charge:
0
Heavy Atom Count:
11
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
293.964g/mol
Monoisotopic Mass:
291.831g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
54A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.2
Literature
| Title | Journal |
|---|---|
| Synthesis and characterization of new donor-acceptor type copolymers based on fluorene derivatives for photovoltaic solar cells. | Journal of nanoscience and nanotechnology 20120701 |
| Synthesis of π-conjugated molecules based on 3,4-dioxypyrroles via Pd-mediated decarboxylative cross-coupling. | The Journal of organic chemistry 20111104 |
| Small band gap polymers synthesized via a modified nitration of 4,7-dibromo-2,1,3-benzothiadiazole. | Organic letters 20101015 |
| Synthesis of cationic conjugated polymers for use in label-free DNA microarrays. | Nature protocols 20060101 |
| Interpolyelectrolyte complexes of conjugated copolymers and DNA: platforms for multicolor biosensors. | Journal of the American Chemical Society 20040225 |
| Synthesis and characterization of new linear pi-conjugated molecules containing bis(ethynylpyridine) units with a benzothiadiazole spacer. | The Journal of organic chemistry 20021101 |
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