| Identification | More | [Name]
5-Methyl-2-thiophenecarboxylic acid | [CAS]
1918-79-2 | [Synonyms]
5-METHYL-2-THENOIC ACID 5-METHYL-2-THIOPHENECARBOXYLIC ACID 5-METHYLTHIOPHENE-2-CARBOXYLIC ACID AKOS B000091 RARECHEM AL BE 0181 TIMTEC-BB SBB004146 2-Carboxy-5-methylthiophene 2-Methyl-5-thiophenecarboxylic acid 2-Thiophenecarboxylic acid, 5-methyl- 5-Methyl-2-thiophenecaroboxylic acid 5-Methylthiophen-2-carboxylic acid 5-Methyl-2-thiopene carboxylic acid 5-METHLY-2-THIOPHENECARBOXYLIC ACID 5-METHYLTHIOPHENE-2-CARBOXYLIC ACID, 98.5% 5-Methylthiophene-2-carboxylic acid, 98+% | [EINECS(EC#)]
217-640-3 | [Molecular Formula]
C6H6O2S | [MDL Number]
MFCD00005439 | [Molecular Weight]
142.18 | [MOL File]
1918-79-2.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust . S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [HazardClass ]
IRRITANT | [HS Code ]
29309090 | [Storage Class]
13 - Non Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
BEIGE CRYSTALLINE POWDER | [Uses]
5-Methyl-2-thiophenecarboxylic acid inhibits the atherosclerotic process in rats and occurs as a volatile constituent of foodstuffs[4]. The compound serves as a ligand coordinating to copper atoms via its carboxylate anions and acts as a precursor in reductions with lithium, ammonia, and ammonium chloride to yield carboxylic acid mixtures for subsequent esterification[5][6]. In oil-containing media, 5-methyl-2-thiophenecarboxylic acid is degraded by the mixed bacterial culture SLPB, with significant reduction observed compared to sterile controls[7]. | [Definition]
ChEBI: 5-Methyl-2-thiophenecarboxylic acid is a thiophenecarboxylic acid. | [Synthesis Reference(s)]
Tetrahedron Letters, 15, p. 2373, 1974 DOI: 10.1016/S0040-4039(01)92259-2 | [Synthesis]
GENERAL PROCEDURE: The general procedure for the synthesis of 5-methyl-2-thiophenecarboxylic acid from 2-acetyl-5-methylthiophene was as follows: Oxone (2 eq.) and trifluoroacetic acid (TFA, 2 eq.) were added to a solution of 2-acetyl-5-methylthiophene (100 mg, 1 eq.) in dioxane (5 mL). The reaction mixture was heated to reflux for 10 hours and subsequently cooled to room temperature. Water (10 mL) was added and the mixture was extracted with ethyl acetate (EtOAc, 2 x 20 mL). The organic layers were combined and washed with saturated sodium bicarbonate (NaHCO3) solution. The sodium bicarbonate solution and the aqueous layer were poured onto crushed ice and acidified with 2 M hydrochloric acid (HCl), at which point a colorless solid precipitated. The precipitate was collected by filtration, dried under vacuum and purified by column chromatography (silica gel; ethyl acetate-hexane, 1:9) to give 5-methyl-2-thiophenecarboxylic acid as a white crystalline solid. Yield: 0.096 g (95% based on 2-acetyl-5-methylthiophene); melting point: 122-123 °C. | [References]
[1] Synthesis (Germany), 2015, vol. 47, # 20, p. 3161 - 3168 [2] Journal of the American Chemical Society, 1947, vol. 69, p. 3096 [3] Recueil des Travaux Chimiques des Pays-Bas, 1949, vol. 68, p. 5,29 |
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