CAS 17228-99-8

2-(4-METHYLPHENYL)-1,3-THIAZOLE-4-CARBOXYLIC ACID

Description:

2-(4-Methylphenyl)-1,3-thiazole-4-carboxylic acid, with the CAS number 17228-99-8, is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features a carboxylic acid functional group, contributing to its acidic properties. The presence of the 4-methylphenyl group enhances its hydrophobic characteristics and may influence its biological activity. Typically, compounds of this nature exhibit moderate solubility in organic solvents and limited solubility in water, which can affect their applications in pharmaceuticals and agrochemicals. The thiazole moiety is often associated with various biological activities, making this compound of interest in medicinal chemistry. Additionally, its structural features may allow for potential interactions with biological targets, leading to various pharmacological effects. Overall, 2-(4-methylphenyl)-1,3-thiazole-4-carboxylic acid represents a class of compounds that can be explored for their chemical reactivity and potential therapeutic applications.

Formula: C₁₁H₉NO₂S

InChI: InChI=1/C11H9NO2S/c1-7-2-4-8(5-3-7)10-12-9(6-15-10)11(13)14/h2-6H,1H3,(H,13,14)/p-1

SMILES: Cc1ccc(cc1)c1nc(cs1)C(=O)[O-]

Synonyms:

• 2-P-Tolyl-Thiazole-4-Carboxylic Acid
• 2-(4-Methylphenyl)-1,3-Thiazole-4-Carboxylate

2-(4-METHYLPHENYL)-1,3-THIAZOLE-4-CARBOXYLIC ACID

CAS: 17228-99-8

Formula: C₁₁H₉NO₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 219.2597

Ref: IN-DA007D5B

2-(p-Tolyl)thiazole-4-carboxylic acid

CAS: 17228-99-8

2-(p-Tolyl)thiazole-4-carboxylic acid

Purity: 97%

Molecular weight: 219.27g/mol

Ref: 54-OR1057268

2-(4-Methylphenyl)-1,3-thiazole-4-carboxylic acid

CAS: 17228-99-8

Formula: C₁₁H₉NO₂S

Purity: 97%

Molecular weight: 219.26

Ref: 10-F217534

2-(4-Methylphenyl)-1,3-thiazole-4-carboxylic acid

CAS: 17228-99-8

2-(4-Methylphenyl)-1,3-thiazole-4-carboxylic acid is a chlorinated compound that has been shown to have anticancer activity. It is structurally modified to increase its potency and has been shown to inhibit cancer cell proliferation in vitro. 2-(4-Methylphenyl)-1,3-thiazole-4-carboxylic acid has been used in the treatment for breast cancer and prostate cancer. This drug also has anticancer effects on the mcf7 cell line, which is an immortalized human mammary epithelial cell line. The mechanism of action of this drug is very similar to that of other anticancer agents: inhibiting DNA synthesis by interfering with DNA replication or by inducing apoptosis.

Formula: C₁₁H₉NO₂S

Purity: Min. 95%

Molecular weight: 219.26 g/mol

Ref: 3D-SAA22899