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方案
99%
表单
liquid
折射率
n20/D 1.563 (lit.)
沸点
192 °C (lit.)
密度
1.172 g/mL at 25 °C (lit.)
官能团
nitrile
SMILES字符串
N#Cc1cccs1
InChI
1S/C5H3NS/c6-4-5-2-1-3-7-5/h1-3H
InChI key
CUPOOAWTRIURFT-UHFFFAOYSA-N
应用
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。
警示用语：
Danger
危险分类
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
127.4 °F - closed cup
闪点(°C)
53 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Muhammad Ajmal et al.
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.
Tülay A Ateşin et al.
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
Ming Yu et al.
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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