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Merck
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文件

T32603

Sigma-Aldrich

2-噻吩甲酸

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號碼:
208-423-4
MDL號碼:
MFCD00005437
分類程式碼代碼:
12352100
PubChem物質ID:
24900123
NACRES:
NA.22

產品線

ReagentPlus®

化驗

99%

bp

260 °C (lit.)

mp

125-127 °C (lit.)

SMILES 字串

OC(=O)c1cccs1

InChI

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

InChI 密鑰

QERYCTSHXKAMIS-UHFFFAOYSA-N

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法律資訊

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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吡咯-2-羧酸 99%

Sigma-Aldrich

P73609

吡咯-2-羧酸

Matthew F McCown et al.
Antimicrobial agents and chemotherapy, 53(5), 2129-2132 (2009-03-11)
In vitro, telaprevir selects subtype-specific resistance pathways for hepatitis C virus GT-1a and GT-1b, as described to have occurred in patients. In GT-1a, the HCV-796 resistance mutation C316Y has low replication capacity (7%) that can be compensated for by the
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
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
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
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
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