About This Item
Fórmula empírica (Notação de Hill):
C5H5IS
Número CAS:
Peso molecular:
224.06
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
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Nível de qualidade
Ensaio
97%
índice de refração
n20/D 1.626 (lit.)
p.e.
81-83 °C/10 mmHg (lit.)
densidade
1.852 g/mL at 25 °C (lit.)
grupo funcional
iodo
temperatura de armazenamento
2-8°C
cadeia de caracteres SMILES
Cc1ccc(I)s1
InChI
1S/C5H5IS/c1-4-2-3-5(6)7-4/h2-3H,1H3
chave InChI
NAZNQEXKAPLVKC-UHFFFAOYSA-N
Descrição geral
2-Iodo-5-methylthiophene is a halogenated thiophene.
Aplicação
2-Iodo-5-methylthiophene may be used for the preparation of:
- methylbis[2-(5-methyl)thienyl]borane
- dimethyl-terthienyl
- 5,5′-dimethy-2,2′-bithienyl
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
192.2 °F - closed cup
Ponto de fulgor (°C)
89 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Chromatographic and spectral characteristics of some polythienyls.
Sease JW and Zechmeister L.
Journal of the American Chemical Society, 69(2), 270-273 (1947)
Synthesis and Properties of Bis (2-heteroaryl) borane Derivatives.
Kohler T, et al.
European Journal of Inorganic Chemistry, 2002(11), 2942-2946 (2002)
Synthesis and pharmacological evaluation of (Z)-9-(heteroarylmethylene)-7-azatricyclo [4.3. 1.0 3, 7] decanes: Thiophene analogues as potent norepinephrine transporter inhibitors.
Zhou J, et al.
Bioorganic & Medicinal Chemistry Letters, 13(20), 3565-3569 (2003)
Alexander Koch et al.
Dalton transactions (Cambridge, England : 2003), 47(36), 12534-12539 (2018-05-05)
The reduction of 2-bromo- and 3-bromothiophene with calcium powder gives impure thienylcalcium complexes due to interference of various subsequent metalation and calcium-halogen exchange reactions as well as ether degradation. Therefore, calcium-iodine exchange succeeds via the reaction of trimethylsilylmethylcalcium halide with
Studies on the Electronic Absorption Spectra of 2, 2'-Bithienyl and Some of Its Derivatives. A Molecular Orbital Treatment.
Abu-Eittah RH and Al-Sugeir FA.
Bulletin of the Chemical Society of Japan, 58(7), 2126-2132 (1985)
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