CAS 102696-70-8

2-Propenoic acid, 3-(3-methyl-2-thienyl)-, (2E)-

Description:

2-Propenoic acid, 3-(3-methyl-2-thienyl)-, (2E)-, also known as a thienyl-substituted acrylic acid, is an organic compound characterized by its unsaturated carboxylic acid structure. It features a propenoic acid backbone with a thienyl group, specifically a 3-methyl-2-thienyl moiety, attached at the third carbon of the double bond. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents and exhibits moderate solubility in water due to the presence of the carboxylic acid functional group. The thienyl substitution can impart unique chemical reactivity and properties, making it of interest in various applications, including polymer synthesis and as a potential building block in organic synthesis. Its reactivity is influenced by the double bond, allowing for various addition reactions. Safety data should be consulted for handling, as it may pose health risks upon exposure. Overall, this compound exemplifies the diversity of organic chemistry and the significance of functional group interactions.

Formula: C₈H₈O₂S

Synonyms:

• (E)-3-(3-methylthiophen-2-yl)acrylic acid
• 2-Propenoic acid, 3-(3-methyl-2-thienyl)-, (2E)-

2-Propenoic acid, 3-(3-methyl-2-thienyl)-, (2E)-

CAS: 102696-70-8

Formula: C₈H₈O₂S

Purity: 96%

Color and Shape: Solid

Molecular weight: 168.2129

Ref: IN-DA00085D

(E)-3-(3-Methylthiophen-2-yl)acrylic acid

CAS: 102696-70-8

(E)-3-(3-Methylthiophen-2-yl)acrylic acid

Purity: 96%

Molecular weight: 168.21292g/mol

Ref: 54-OR79694

(E)-3-(3-methylthiophen-2-yl)acrylic acid

CAS: 102696-70-8

Purity: 96%

Molecular weight: 168.2100067

Ref: 10-F872496

(2E)-3-(3-Methylthiophen-2-yl)prop-2-enoic acid

CAS: 102696-70-8

(2E)-3-(3-Methylthiophen-2-yl)prop-2-enoic acid is a naturally occurring compound with two stereoisomers, the cis and trans isomers. The cis isomer has been found to have the same physiological properties as pyrantel, while the trans isomer has been shown to be resistant to alkaline hydrolysis. (2E)-3-(3-Methylthiophen-2-yl)prop-2-enoic acid can be isolated from plants by using chromatographic techniques that separate it from other compounds with similar structures. This compound also has a homolog, (4R)-4-(3,5,-dimethylphenyl)butanoic acid, which can be synthesized in the laboratory.

Formula: C₈H₈O₂S

Purity: Min. 95%

Molecular weight: 168.21 g/mol

Ref: 3D-CEA69670