CAS 106392-48-7

2-Propenamide, 2-cyano-3-(4-hydroxy-3,5-bis(1-methylethyl)phenyl)-

Description:

2-Propenamide, 2-cyano-3-(4-hydroxy-3,5-bis(1-methylethyl)phenyl)-, also known by its CAS number 106392-48-7, is an organic compound characterized by its amide functional group and a cyano group attached to a propenamide backbone. This compound features a phenolic structure with two isopropyl groups at the 3 and 5 positions, contributing to its hydrophobic characteristics and potential biological activity. The presence of the hydroxyl group enhances its solubility in polar solvents and may influence its reactivity and interaction with biological systems. The compound is likely to exhibit properties typical of amides, such as moderate polarity and the ability to participate in hydrogen bonding. Its structural complexity suggests potential applications in pharmaceuticals or as an intermediate in organic synthesis. However, specific data regarding its stability, reactivity, and toxicity would require further investigation through experimental studies or literature review.

Formula: C₁₆H₂₀N₂O₂

InChI: InChI=1/C16H20N2O2/c1-9(2)13-6-11(5-12(8-17)16(18)20)7-14(10(3)4)15(13)19/h5-7,9-10,19H,1-4H3,(H2,18,20)/b12-5+

Synonyms:

• St 271
• (2E)-2-cyano-3-[4-hydroxy-3,5-bis(1-methylethyl)phenyl]prop-2-enamide

2-Propenamide, 2-cyano-3-(4-hydroxy-3,5-bis(1-methylethyl)phenyl)-

CAS: 106392-48-7

Formula: C₁₆H₂₀N₂O₂

Purity: 99%

Color and Shape: Solid

Molecular weight: 272.3422

Ref: IN-DA009T7L

ST271

CAS: 106392-48-7

ST271

Purity: ≥95%

Molecular weight: 272.34g/mol

Ref: 54-BUP05938

ST271

CAS: 106392-48-7

ST271 is an effective protein tyrosine kinase (PTK) inhibitor.

Formula: C₁₆H₂₀N₂O₂

Purity: 98.94%

Color and Shape: Solid

Molecular weight: 272.34

Ref: TM-T4511

(E)-2-CYANO-3-(4-HYDROXY-3,5-DIISOPROPYLPHENYL)ACRYLAMIDE

CAS: 106392-48-7

Purity: 99%

Molecular weight: 272.3479919

Ref: 10-F832641

ST271

CAS: 106392-48-7

ST271 is a novel, potent and selective inhibitor of bacterial DNA-dependent RNA polymerase. It has been shown to be active against Gram-positive bacteria that are resistant to ceftriaxone and erythromycin, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci (VRE). ST271 blocks the synthesis of proteins by inhibiting the enzyme ribosome. This drug also has anti-inflammatory properties, which may be due to its ability to inhibit epidermal growth factor receptor phosphorylation.

Formula: C₁₆H₂₀N₂O₂

Purity: Min. 95%

Molecular weight: 272.34 g/mol

Ref: 3D-GEA39248