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T32603

2-噻吩甲酸

Name: 2-噻吩甲酸
Brand: ALDRICH

ReagentPlus^®, 99%

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About This Item

经验公式（希尔记法）:

C₅H₄O₂S

CAS号:

527-72-0

分子量:

128.15

Beilstein:

110150

EC 号:

208-423-4

MDL编号:

MFCD00005437

UNSPSC代码:

12352100

PubChem化学物质编号:

24900123

NACRES:

NA.22

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双（频哪醇合）二硼

质量水平

100

产品线

ReagentPlus^®

方案

99%

沸点

260 °C (lit.)

mp

125-127 °C (lit.)

SMILES字符串

OC(=O)c1cccs1

InChI

1S/C5H4O2S/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7)

InChI key

QERYCTSHXKAMIS-UHFFFAOYSA-N

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法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Deconstructing fragment-based inhibitor discovery.

Kerim Babaoglu et al.

Nature chemical biology, 2(12), 720-723 (2006-10-31)

Fragment-based screens test multiple low-molecular weight molecules for binding to a target. Fragments often bind with low affinities but typically have better ligand efficiencies (DeltaG(bind)/heavy atom count) than traditional screening hits. This efficiency, combined with accompanying atomic-resolution structures, has made

Discovery of thiophene-2-carboxylic acids as potent inhibitors of HCV NS5B polymerase and HCV subgenomic RNA replication. Part 2: tertiary amides.

Laval Chan et al.

Bioorganic & medicinal chemistry letters, 14(3), 797-800 (2004-01-27)

Further SAR studies on the thiophene-2-carboxylic acids are reported. These studies led to the identification of a series of tertiary amides that show inhibition of both HCV NS5B polymerase in vitro and HCV subgenomic RNA replication in Huh-7 cells. Structural

Stereocontrolled synthesis of α-amino-α'-alkoxy ketones by a copper-catalyzed cross-coupling of peptidic thiol esters and α-alkoxyalkylstannanes.

Hao Li et al.

Organic letters, 13(14), 3682-3685 (2011-06-17)

A stereocontrolled synthesis of α-amino-α'-alkoxy ketones is described. This pH-neutral copper(I) thiophene-2-carboxylate (CuTC)-catalyzed cross-coupling of amino acid thiol esters and chiral nonracemic α-alkoxyalkylstannanes gives α-amino-α'-alkoxy ketones in good to excellent yields with complete retention of configuration at the α-amino- and

Nonbasic, room temperature, palladium-catalyzed coupling of aryl and alkenyl iodides with boronic acids mediated by copper(I) thiophene-2-carboxylate (CuTC).

C Savarin et al.

Organic letters, 3(14), 2149-2152 (2001-07-07)

[reaction: see text] A new protocol for the palladium-catalyzed, copper-mediated coupling of aryl and alkenyl iodides with boronic acids is described. As an alternative to the well-known and widely used Suzuki cross-coupling, this reaction occurs in the absence of a

Discovery of thiophene-2-carboxylic acids as potent inhibitors of HCV NS5B polymerase and HCV subgenomic RNA replication. Part 1: Sulfonamides.

Laval Chan et al.

Bioorganic & medicinal chemistry letters, 14(3), 793-796 (2004-01-27)

The discovery of a novel class of HCV NS5B polymerase inhibitors, 3-arylsulfonylamino-5-phenyl-thiophene-2-carboxylic acids is described. SAR studies have yielded several potent inhibitors of HCV polymerase as well as of HCV subgenomic RNA replication in Huh-7 cells.

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2-噻吩甲酸