247766
3-チオフェンカルボン酸
99%
別名:
β-Thiophenecarboxylic acid, β-Thiophenic acid, 3-Carboxythiophene, 3-Thenoic acid, 3-Thienylcarboxylic acid, Thiophene-3-carboxylic acid
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すべての画像(3)
About This Item
実験式（ヒル表記法）:
C5H4O2S
CAS番号:
分子量:
128.15
Beilstein:
1994
EC Number:
MDL番号:
UNSPSCコード:
12352100
PubChem Substance ID:
NACRES:
NA.22
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品質水準
アッセイ
99%
mp
136-141 °C (lit.)
溶解性
water: soluble 0.2 g/10 mL, clear to almost clear, colorless to slightly brownish-yellow
官能基
carboxylic acid
SMILES記法
OC(=O)c1ccsc1
InChI
1S/C5H4O2S/c6-5(7)4-1-2-8-3-4/h1-3H,(H,6,7)
InChI Key
YNVOMSDITJMNET-UHFFFAOYSA-N
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関連するカテゴリー
詳細
Mechanism of photopolymerization of 3-thiophenecarboxylic acid catalyzed by potassium dichromate has been reported.
アプリケーション
3-Thiophenecarboxylic acid has been used in the preparation of:
- novel acetylene monomer, required for the synthesis of poly(2-methylbut-2-enyl thiophene-3-carboxylate)
- oxazolines and oxazoles
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
Eyeshields, Gloves, type N95 (US)
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
247766-VAR:
247766-1G:
247766-BULK:
247766-250MG:
247766-5G:
Sergey A Piletsky et al.
Chemical communications (Cambridge, England), (19)(19), 2222-2223 (2004-10-07)
A novel method of photochemical polymerization of thiophene derivatives in aqueous solution catalyzed by potassium dichromate and initiated by illumination is described.
Katherine L Wozniak et al.
The Journal of general physiology, 150(9), 1239-1248 (2018-07-18)
The prevention of polyspermy is essential for the successful progression of normal embryonic development in most sexually reproducing species. In external fertilizers, the process of fertilization induces a depolarization of the egg's membrane within seconds, which inhibits supernumerary sperm from
D A Heerding et al.
Bioorganic & medicinal chemistry letters, 11(16), 2061-2065 (2001-08-22)
1,4-Disubstituted imidazole inhibitors of Staphylococcus aureus and Escherichia coli enoyl acyl carrier protein reductase (FabI) have been identified. Crystal structure data shows the inhibitor 1 bound in the enzyme active site of E. coli FabI.
H Zejli et al.
Talanta, 185, 513-519 (2018-05-16)
This work demonstrates the development of electrochemical aptasensor using ochratoxin A (OTA) aptamers. Different aptamer coupling strategies were tested using polythiophene-carboxylic acid (PT3C) and polypyrrole-3-carboxylic acid (PP3C). The best sensitivity was recorded by polythiophene-3-carboxylic acid (PT3C) on screen-printed carbon electrode
Banu Koz et al.
International journal of molecular sciences, 9(3), 383-393 (2009-03-28)
A new polyacetylene derivative with electroactive thiophene substituent, namely poly(2-methylbut-2-enyl thiophene-3-carboxylate) was synthesized and characterized. For this purpose, novel acetylene monomer was synthesized by the reaction of 3-thiophenecarboxylic acid with propargyl bromide and polymerized with a Rh catalyst to give
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