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Merck
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Key Documents

154385

Sigma-Aldrich

2-噻吩甲腈

99%

同義詞:

2-氰基噻吩, 噻吩-2-甲腈

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About This Item

經驗公式(希爾表示法):
C5H3NS
CAS號碼:
分子量::
109.15
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

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.)

官能基

nitrile

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


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分析證明 (COA)

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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.
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
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.

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