Methyl 2-aminothiophene-3-carboxylate

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Methyl 2-aminothiophene-3-carboxylate

  • NameMethyl 2-aminothiophene-3-carboxylate
  • CAS4651-81-4
  • Purity99%
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Product Details

Manufacturers supply cost-effective and customizable Methyl 2-aminothiophene-3-carboxylate 4651-81-4

  • Molecular Formula:C6H7NO2S
  • Molecular Weight:157.193
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:0.013mmHg at 25°C 
  • Melting Point:76-81 °C(lit.) 
  • Refractive Index:1.598 
  • Boiling Point:259.451 °C at 760 mmHg 
  • PKA:0.10±0.10(Predicted) 
  • Flash Point:110.712 °C 
  • PSA:80.56000 
  • Density:1.32 g/cm3 
  • LogP:1.69810 

Methyl 2-aminothiophene-3-carboxylate(Cas 4651-81-4) Usage

InChI:InChI=1/C6H7NO2S/c1-9-6(8)4-2-3-10-5(4)7/h2-3H,7H2,1H3

4651-81-4 Relevant articles

Design, synthesis, molecular docking and cytotoxic activity of novel urea derivatives of 2-amino-3-carbomethoxythiophene

Amperayani, Karteek Rao,Parimi, Umadevi,Penumutchu, Srinivasa R,Thangudu, Suresh,Vankayala, Raviraj,Vikram, Venugopalarao

, (2020)

Abstract: An efficient feasible route fo...

Design, synthesis, docking, molecular dynamics and bioevaluation studies on novel N-methylpicolinamide and thienopyrimidine derivatives with inhibiting NF-κB and TAK1 activities: Cheminformatics tools RDKit applied in drug design

Tan, Ninghua,Wang, Linxiao,Wang, Zhe,Zhang, Qian,Zhu, Wufu

, (2021/07/09)

Using cheminformatics tools RDKit and li...

Synthesis of novel 2-(1-adamantanylcarboxamido)thiophene derivatives. Selective cannabinoid type 2 (CB2) receptor agonists as potential agents for the treatment of skin inflammatory disease

Mugnaini, Claudia,Rabbito, Alessandro,Brizzi, Antonella,Palombi, Nastasja,Petrosino, Stefania,Verde, Roberta,Di Marzo, Vincenzo,Ligresti, Alessia,Corelli, Federico

, p. 239 - 251 (2018/10/24)

A set of CB2R ligands, based on the thio...

Iridium complex containing thieno-[2,3-d] pyrimidine group and application in electroluminescence device

-

Paragraph 0044-0047, (2018/03/09)

The invention disclose an iridium comple...

4651-81-4 Process route

1,4-dithiane-2,5-diol
40018-26-6

1,4-dithiane-2,5-diol

methyl 2-cyanoacetate
105-34-0

methyl 2-cyanoacetate

Methyl 2-aminothiophene-3-carboxylate
4651-81-4

Methyl 2-aminothiophene-3-carboxylate

Conditions
Conditions Yield
With triethylamine; N,N-dimethyl-formamide; In methanol; at 50 ℃; for 0.05h; Sealed tube; Microwave irradiation; Inert atmosphere;
94%
With triethylamine; In methanol; at 0 - 40 ℃;
86%
With triethylamine; N,N-dimethyl-formamide; In methanol; at 50 ℃; for 0.0333333h; microwave irradiation;
82%
With triethylamine; In methanol; at 0 - 60 ℃;
78%
With triethylamine; In methanol; at -5 - 40 ℃; for 4h;
77%
With triethylamine; In DMF (N,N-dimethyl-formamide); at 0 - 20 ℃; for 2h;
68%
With triethylamine; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 3h;
64%
With triethylamine; In N,N-dimethyl-formamide; at 25 - 45 ℃; for 2.16667h;
58%
With triethylamine; In N,N-dimethyl-formamide; at 25 ℃; for 0.166667h;
58%
With triethylamine; In N,N-dimethyl-formamide; at 45 ℃; for 0.5h;
55%
With triethylamine; In methanol; at 0 - 40 ℃; for 2.5h;
44%
With triethylamine;
With acetic acid; triethylamine; In N,N-dimethyl-formamide;
methanol
67-56-1

methanol

2-aminothiophene-3-carboxylic acid
56387-08-7

2-aminothiophene-3-carboxylic acid

Methyl 2-aminothiophene-3-carboxylate
4651-81-4

Methyl 2-aminothiophene-3-carboxylate

Conditions
Conditions Yield
With thionyl chloride; at 0 ℃;

4651-81-4 Upstream products

  • 40018-26-6
    40018-26-6

    1,4-dithiane-2,5-diol

  • 105-34-0
    105-34-0

    methyl 2-cyanoacetate

  • 75-07-0
    75-07-0

    acetaldehyde

  • 53982-98-2
    53982-98-2

    2-cyano-but-2-enoic acid methyl ester

4651-81-4 Downstream products

  • 14080-50-3
    14080-50-3

    thieno[2,3-d]pyrimidin-4(3H)one

  • 18740-38-0
    18740-38-0

    1H-thieno[2,3-d]pyrimidine-2,4-dione

  • 126637-07-8
    126637-07-8

    methyl 2-isothiocyanato-thiophene-3-carboxylate

  • 2125-85-1
    2125-85-1

    3-hydroxypyrazolo<3,4-c>pyridazine

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