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化驗
99%
形狀
liquid
折射率
n20/D 1.563 (lit.)
bp
192 °C (lit.)
密度
1.172 g/mL at 25 °C (lit.)
SMILES 字串
N#Cc1cccs1
InChI
1S/C5H3NS/c6-4-5-2-1-3-7-5/h1-3H
InChI 密鑰
CUPOOAWTRIURFT-UHFFFAOYSA-N
應用
2-噻吩腈(2-氰基噻吩)可用于制备 thiaplatinacycles。它也用于合成 2,2′-噻吩基吡咯。
訊號詞
Danger
危險分類
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
127.4 °F - closed cup
閃點(°C)
53 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Inorganic chemistry, 47(11), 4596-4604 (2008-05-02)
The reaction of 2-cyanothiophene with a zerovalent platinum bisalkylphosphine fragment yields two thiaplatinacycles derived from the cleavage of the substituted and unsubstituted C-S bonds. While cleavage away from the cyano group is preferred kinetically, cleavage adjacent to the cyano group
Journal of colloid and interface science, 470, 39-46 (2016-03-02)
In this study, the synthesis of micron-sized poly(vinylbenzyl chloride) (p(VBC)) beads and subsequent conversion of the reactive chloromethyl groups to double amidoxime group containing moieties by post modification is reported. The prepared beads were characterized by SEM and FT-IR spectroscopy.
Organic letters, 6(6), 1057-1059 (2004-03-12)
[reaction: see text] Two new series of 2,2'-bipyrroles and 2,2'-thienylpyrroles have been prepared by trimethylsilyl trifluoromethanesulfonate (TMSOTf)-mediated reaction of donor-acceptor cyclopropanes with 2-cyanopyrroles and 2-cyanothiophene, respectively. This method opens the door toward a wide variety of unsymmetrical bipyrroles and thienylpyrroles.
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