| | Identification | More |  | [Name] 
 3-Chlorothiophene-2-carboxylic acid
 |  | [CAS] 
 59337-89-2
 |  | [Synonyms] 
 3-CHLOROTHIOPHENE-2-CARBOXYLIC ACID
 AKOS 93295
 BUTTPARK 29\06-43
 RARECHEM AL BE 1228
 TIMTEC-BB SBB003936
 3-Chlorothiophene-2-carboxylic acid 98%
 3-Chlorothiophene-2-carboxylicacid98%
 3-Chlorothiophene-2-carboxylic acid ,99%
 |  | [EINECS(EC#)] 
 275-581-9
 |  | [Molecular Formula] 
 C5H3ClO2S
 |  | [MDL Number] 
 MFCD00043888
 |  | [Molecular Weight] 
 162.59
 |  | [MOL File] 
 59337-89-2.mol
 | 
 | Chemical Properties | Back Directory |  | [Appearance] 
 white to light yellow crystal powder
 |  | [Melting point ] 
 186-190 °C (lit.)
 |  | [Boiling point ] 
 291.7±20.0 °C(Predicted)
 |  | [density ] 
 1.466 (estimate)
 |  | [storage temp. ] 
 2-8°C
 |  | [solubility ] 
 DMSO (Sparingly), Methanol (Slightly)
 |  | [form ] 
 solid
 |  | [pka] 
 3.09±0.10(Predicted)
 |  | [color ] 
 White to Off-White
 |  | [Detection Methods] 
 HPLC
 |  | [BRN ] 
 121052
 |  | [InChI] 
 InChI=1S/C5H3ClO2S/c6-3-1-2-9-4(3)5(7)8/h1-2H,(H,7,8)
 |  | [InChIKey] 
 BXEAAHIHFFIMIE-UHFFFAOYSA-N
 |  | [SMILES] 
 C1(C(O)=O)SC=CC=1Cl
 |  | [CAS DataBase Reference] 
 59337-89-2(CAS DataBase Reference)
 | 
 | Safety Data | Back Directory |  | [Hazard Codes ] 
 Xi
 |  | [Risk Statements ] 
 R36/37/38:Irritating to eyes, respiratory system and skin .
 |  | [Safety Statements ] 
 S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
 S36:Wear suitable protective clothing .
 S24/25:Avoid contact with skin and eyes .
 |  | [WGK Germany ] 
 3
 
 |  | [Hazard Note ] 
 Irritant
 |  | [HS Code ] 
 29349990
 | 
 | Hazard Information | Back Directory |  | [Chemical Properties] 
 white to light yellow crystal powder
 |  | [Uses] 
 
 3-Chlorothiophene-2-carboxylic acid may be used in the synthesis of 3-chloro-N-[(4-chlorophenyl)(methyl)carbamothioyl]thiophene-2-carboxamide. |  | [Synthesis] 
 
 GENERAL STEPS: Methyl 3-chlorothiophene-2-carboxylate (50 g, 0.28 mol) was dissolved in methanol (100 mL), aqueous sodium hydroxide solution (2M, 400 mL) was added slowly, and the reaction temperature was maintained at 0 °C. The reaction mixture was stirred at room temperature for 2 hours. After removal of methanol by distillation under reduced pressure, the aqueous phase was washed with ether and subsequently acidified with 2N hydrochloric acid to pH < 3. The precipitated white solid was collected by filtration and dried under vacuum to give 3-chlorothiophene-2-carboxylic acid (45 g, 98% yield). Mass spectrometry (MS) analysis showed a molecular ion peak (M+H+) of 163. |  | [References] 
 [1] Heterocycles,  1985,  vol. 23,  # 6,  p. 1431 - 1435
 [2] Patent: WO2012/139425,  2012,  A1. Location in patent: Page/Page column 119
 [3] Heterocycles,  2007,  vol. 71,  # 1,  p. 87 - 104
 [4] Patent: WO2013/28670,  2013,  A1. Location in patent: Page/Page column 96
 [5] Patent: US9181236,  2015,  B2. Location in patent: Page/Page column 107
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