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Merck
CN

154385

2-噻吩甲腈

99%

别名:

2-氰基噻吩, 噻吩-2-甲腈

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关于此项目

经验公式(希尔记法):
C5H3NS
化学文摘社编号:
分子量:
109.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
213-706-0
MDL number:
Assay:
99%
Form:
liquid
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产品名称

2-噻吩甲腈, 99%

InChI key

CUPOOAWTRIURFT-UHFFFAOYSA-N

InChI

1S/C5H3NS/c6-4-5-2-1-3-7-5/h1-3H

SMILES string

N#Cc1cccs1

assay

99%

form

liquid

refractive index

n20/D 1.563 (lit.)

bp

192 °C (lit.)

density

1.172 g/mL at 25 °C (lit.)

functional group

nitrile

Quality Level

Application

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

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

127.4 °F - closed cup

flash_point_c

53 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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.
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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