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2-Thiophenecarboxylic acid

  • Product Name: 2-Thiophenecarboxylic acid
  • CasNo: 527-72-0
  • Purity:
  • Appearance: white to light yellow crystal powder

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CasNo: 527-72-0

Molecular Formula: C5H4O2S

Appearance: white to light yellow crystal powder

Chinese Manufacturer Supply 527-72-0 with Cheapest Price, Buy High Grade 2-Thiophenecarboxylic acid

  • Molecular Formula:C5H4O2S
  • Molecular Weight:128.152
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:0.00639mmHg at 25°C 
  • Melting Point:125-127 °C(lit.) 
  • Refractive Index:1.5160 (estimate) 
  • Boiling Point:260 °C at 760 mmHg 
  • PKA:3.49(at 25℃) 
  • Flash Point:117.8 °C 
  • PSA:65.54000 
  • Density:1.401 g/cm3 
  • LogP:1.44630 

2-Thiophenecarboxylic acid(Cas 527-72-0) Usage

Uses

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.

Chemical Properties

white to light yellow crystal powder

Synthesis Reference(s)

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

Consumer Uses

ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C5H4O2S/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7)/p-1

527-72-0 Relevant articles

LIQUID-PHASE CATALYTIC OXIDATION OF 2-METHOXYMETHYLTHIOPHENE

Leichenko, A. A.,Schedrinskaya, T. V.,Volkov, M. N.

, p. 714 - 718 (1980)

The oxidation of 2-methoxymethylthiophen...

CLEAVAGE DIRECTION OF C-O BOND IN ANION RADICALS OF METHYL ESTERS OF AROMATIC ACIDS IN APROTIC SOLVENTS

Gul'tai, V. P.,Rubinskaya, T. Ya.,Korotaeva, L. M.

, p. 1499 - 1500 (1982)

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Facile production of vitamin B3 and other heterocyclic carboxylic acids using an efficient Ag/ZnO/graphene-Si hybrid nanocatalyst

Attia, Yasser A.,Vázquez, Carlos Vázquez,Mohamed, Yasser M. A.

, p. 203 - 218 (2017)

Abstract: High yield of vitamin B3 is pr...

Palladium-promoted One-step Carboxylation of Aromatic Compounds with Carbon Monoxide

Fujiwara, Yuzo,Kawauchi, Tomio,Taniguchi, Hiroshi

, p. 220 - 221 (1980)

The one-step carboxylation of aromatic c...

Structure and Mechanism of Pseudomonas aeruginosa PA0254/HudA, a prFMN-Dependent Pyrrole-2-carboxylic Acid Decarboxylase Linked to Virulence

Payne, Karl A. P.,Marshall, Stephen A.,Fisher, Karl,Rigby, Stephen E. J.,Cliff, Matthew J.,Spiess, Reynard,Cannas, Diego M.,Larrosa, Igor,Hay, Sam,Leys, David

, p. 2865 - 2878 (2021)

The UbiD family of reversible (de)carbox...

Gram-scale synthesis of carboxylic acids via catalytic acceptorless dehydrogenative coupling of alcohols and hydroxides at an ultralow Ru loading

Chen, Cheng,Cheng, Hua,Verpoort, Francis,Wang, Zhi-Qin,Wu, Zhe,Yuan, Ye,Zheng, Zhong-Hui

, (2021/12/13)

Acceptorless dehydrogenative coupling (A...

Transformation of Thioacids into Carboxylic Acids via a Visible-Light-Promoted Atomic Substitution Process

Fu, Qiang,Liang, Fu-Shun,Lou, Da-Wei,Pan, Gao-Feng,Wang, Rui,Wu, Min,Xie, Kai-Jun

supporting information, p. 2020 - 2024 (2022/03/31)

A visible-light-promoted atomic substitu...

Photoinduced FeCl3-Catalyzed Alkyl Aromatics Oxidation toward Degradation of Polystyrene at Room Temperature?

Zhang, Guoxiang,Zhang, Zongnan,Zeng, Rong

supporting information, p. 3225 - 3230 (2021/09/28)

While polystyrene is widely used in dail...

527-72-0 Process route

C<sub>15</sub>H<sub>16</sub>O<sub>2</sub>S
1309453-50-6

C15H16O2S

2-thiophenylcarboxylic acid
527-72-0

2-thiophenylcarboxylic acid

[2-(4-methoxy-phenyl)-cyclopropyl]-thiophen-2-yl-methanone
75021-56-6

[2-(4-methoxy-phenyl)-cyclopropyl]-thiophen-2-yl-methanone

4-methoxybenzoic acid
100-09-4

4-methoxybenzoic acid

Conditions
Conditions Yield
C15H16O2S; With oxygen; sodium hydride; In tetrahydrofuran; at 0 - 20 ℃; for 11h;
With hydrogenchloride; In water;
90%
10%
10%
C<sub>15</sub>H<sub>15</sub>NOS
443895-69-0

C15H15NOS

2-thiophenylcarboxylic acid
527-72-0

2-thiophenylcarboxylic acid

C<sub>6</sub>H<sub>4</sub>NCH<sub>2</sub>CHCCH<sub>2</sub>
491-35-0

C6H4NCH2CHCCH2

C<sub>15</sub>H<sub>14</sub>N<sub>2</sub>O<sub>2</sub>S
1370460-32-4

C15H14N2O2S

Conditions
Conditions Yield
With trifluoroacetic acid; sodium nitrite; In chloroform; at 0 - 5 ℃; for 1h;
54%

527-72-0 Upstream products

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    thiophene

  • 30930-49-5
    30930-49-5

    bis(2-thiophenecarbonyl) peroxide

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    1003-09-4

    2-bromothiophene

  • 925-90-6
    925-90-6

    ethylmagnesium bromide

527-72-0 Downstream products

  • 5380-42-7
    5380-42-7

    thiophene-2-carboxylic acid methyl ester

  • 59303-19-4
    59303-19-4

    propyl thiophene‐2‐carboxylate

  • 2810-04-0
    2810-04-0

    Ethyl thiophene-2-carboxylate

  • 35250-80-7
    35250-80-7

    thiophene-2-carboxylic acid isopentyl ester

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