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2-Thiophenecarboxylic acid

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2-Thiophenecarboxylic acid Basic information

Product Name:
2-Thiophenecarboxylic acid
Synonyms:
  • 2-Thenoic Acid 2-Thiophenic Acid Thiophene-2-carboxylic acid
  • LABOTEST-BB LT02016392
  • AKOS B022791
  • AKOS BBS-00003739
  • ALPHA-THENOIC ACID
  • 2-THENOIC ACID
  • 2-THIOPHENIC ACID
  • 2-THIOPHENECARBOXYLIC ACID
CAS:
527-72-0
MF:
C5H4O2S
MW:
128.15
EINECS:
208-423-4
Product Categories:
  • Building Blocks
  • C4 to C6
  • Heterocyclic Compounds
  • Miscellaneous
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Thiophenes
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Thiophene&Benzothiophene
  • Organic acids
  • Building Blocks
  • Heterocyclic Building Blocks
Mol File:
527-72-0.mol
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2-Thiophenecarboxylic acid Chemical Properties

Melting point:
125-127 °C(lit.)
Boiling point:
260 °C(lit.)
Density 
1.42
refractive index 
1.5160 (estimate)
Flash point:
259-261°C
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Acetone (Slightly), Chloroform (Slightly)
form 
solid
pka
3.49(at 25℃)
color 
White to Off-White
Water Solubility 
80 g/L (20 ºC)
Merck 
14,9354
BRN 
110150
InChIKey
QERYCTSHXKAMIS-UHFFFAOYSA-N
LogP
1.570
CAS DataBase Reference
527-72-0(CAS DataBase Reference)
NIST Chemistry Reference
2-Thiophenecarboxylic acid(527-72-0)
EPA Substance Registry System
2-Thiophenecarboxylic acid (527-72-0)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
XM8330200
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29349990

MSDS

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2-Thiophenecarboxylic acid Usage And Synthesis

Chemical Properties

The substance is a light yellow crystal powder. It dissolves in hot water, ethanol, and ether, and is only slightly soluble in chloroform.

Uses

2-Thenoic Acid, is a sulfur-containing heterocyclic compound, used in the synthesis of pharmaceutical and biologically active compounds. It is also shown to be utilized by presumptive Rhodococcus bacterium in soil, as a sole source of carbon.

Production Methods

Thiophene 2-Carboxylic Acid, T2CA, is prepared via oxidation of 2-acetylthiophene using hypochlorite, because oxidation of alkylthiophenes leads to general breakdown of the thiophene ring.

Definition

ChEBI: Thiophene-2-carboxylic acid is a thiophenecarboxylic acid in which the carboxy group is located at position 2. It is a conjugate acid of a thiophene-2-carboxylate.

Application

The sodium salt of 2-Thiophenecarboxylic acid(T2CA) is used to treat influenza (trophires). Other salts, e.g., the Li salt, have minor medicinal uses and the free acid is a mucolytic. A US Patent describes the use of the Na salt as a lubricating oil thickener. ?Suprofen, a nonsteroidal anti-inflammatory (NSAI), and tienilic acid (ticrynafen), a potent diuretic, were both very large prospective markets for T2CA or its acid chloride, but were almost completely withdrawn in the 1980s. Sanofi Aventis'NSAI tiaprofenic acid was comparatively successful in this market, but although it is still marketed it has subsequently been superceded by alternative products. The 5-nitro derivative of T2CA is used to produce nifurzide, an intestinal antibacterial. Pfizer's anti-inflammatory tenidap is a developing drug which uses the acid chloride of T2CA as the starting intermediate.

Synthesis Reference(s)

The Journal of Organic Chemistry, 30, p. 3520, 1965 DOI: 10.1021/jo01021a055

Purification Methods

Crystallise the acid from water and dry it in a vacuum. The amide has m 181o(from H2O) and pK2 5 10.54(50% aqueous dioxane). [Beilstein 18 H 289, 18 I 438, 18 II 269, 18 III/IV 4011, 18/6 V 158.]

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