CAS 105558-72-3

3-Thiophenecarbonitrile, 2-amino-4-ethoxy-

Description:

3-Thiophenecarbonitrile, 2-amino-4-ethoxy- is an organic compound characterized by the presence of a thiophene ring, a cyano group, and an ethoxy substituent. The thiophene ring contributes to its aromatic properties, while the cyano group (-C≡N) introduces significant polarity and reactivity, making it a potential candidate for various chemical reactions, including nucleophilic additions. The amino group (-NH2) enhances its basicity and can participate in hydrogen bonding, influencing its solubility and reactivity. The ethoxy group (-OCH2CH3) adds steric bulk and can affect the compound's overall lipophilicity. This compound may exhibit interesting biological activities due to its structural features, making it of interest in medicinal chemistry and material science. Its synthesis and characterization would typically involve standard organic reactions, and its properties can be further explored through spectroscopic techniques. Overall, 3-Thiophenecarbonitrile, 2-amino-4-ethoxy- presents a unique combination of functional groups that can be leveraged in various chemical applications.

Formula: C₇H₈N₂OS

2-Amino-4-ethoxythiophene-3-carbonitrile

CAS: 105558-72-3

Formula: C₇H₈N₂OS

Purity: 95%

Color and Shape: Solid

Molecular weight: 168.2162

Ref: IN-DA01A2SC

2-Amino-4-ethoxythiophene-3-carbonitrile

CAS: 105558-72-3

Formula: C₇H₈N₂OS

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 168.21

Ref: 10-F547130

2-Amino-4-ethoxythiophene-3-carbonitrile

CAS: 105558-72-3

2-Amino-4-ethoxythiophene-3-carbonitrile is a chemical compound that contains an orthoacetate group, which is an acetyl group in the 2 position and an ethoxy group in the 4 position. It is used in organic synthesis as a building block for introducing orthoalkoxysubstituents into ring systems. This compound can be prepared by transesterification of trimethylorthoacetate with 2-aminoethanethiol followed by reduction of the nitrile to amine with zinc dust and hydrochloric acid. The trimethylorthoacetate can be prepared by reacting methyltriphenylphosphonium bromide with trimethyl orthoformate and potassium hydroxide. This reaction has been shown to be efficient and high yielding.

Formula: C₇H₈N₂OS

Purity: Min. 95%

Molecular weight: 168.22 g/mol

Ref: 3D-FEA55872