CAS 105512-81-0

4-(3-BROMO-PHENYL)-THIAZOL-2-YLAMINE

Description:

4-(3-Bromo-phenyl)-thiazol-2-ylamine is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. The presence of a bromo substituent on the phenyl group enhances its reactivity and can influence its biological activity. This compound typically exhibits properties such as moderate solubility in organic solvents and potential interactions with biological targets, making it of interest in medicinal chemistry. The thiazole moiety is known for its role in various pharmacological activities, including antimicrobial and anticancer properties. Additionally, the amine functional group contributes to its basicity and potential for forming hydrogen bonds, which can affect its interaction with other molecules. The compound's structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in synthetic organic chemistry. Overall, 4-(3-bromo-phenyl)-thiazol-2-ylamine is a compound of interest for further research in both synthetic and medicinal chemistry contexts.

Formula: C₉H₇BrN₂S

InChI: InChI=1/C9H7BrN2S/c10-7-3-1-2-6(4-7)8-5-13-9(11)12-8/h1-5H,(H2,11,12)

SMILES: c1cc(cc(c1)Br)c1csc(=N)[nH]1

Synonyms:

• Buttpark 41\03-41
• Aurora 22596
• Art-Chem-Bb B000319
• 4-(3-Bromophenyl)-1,3-Thiazol-2-Amine
• 4-(3-Bromophenyl)-1,3-Thiazole-2-Ylamine
• Akos B000319
• Akos Bbs-00008008

4-(3-bromophenyl)thiazol-2-amine

CAS: 105512-81-0

Formula: C₉H₇BrN₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 255.1343

Ref: IN-DA003GE3

4-(3-Bromophenyl)-1,3-thiazol-2-amine

CAS: 105512-81-0

4-(3-Bromophenyl)-1,3-thiazol-2-amine

Purity: ≥95%

Molecular weight: 255.13g/mol

Ref: 54-OR311065

4-(3-Bromophenyl)-1,3-thiazol-2-amine

CAS: 105512-81-0

4-(3-Bromophenyl)-1,3-thiazol-2-amine is an inhibitor of enzymes such as cholinesterase and covalent binding. It has been shown to inhibit the activity of cholinesterase in vitro. This drug is not active against erythromycin or lincomycin. 4-(3-Bromophenyl)-1,3-thiazol-2-amine also has a phenylthiazole linkage that can be conjugated with other molecules for use as a therapeutic agent.

Formula: C₉H₇BrN₂S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 255.14 g/mol

Ref: 3D-FB112294

4-(3-Bromo-phenyl)-thiazol-2-ylamine

CAS: 105512-81-0

Formula: C₉H₇BrN₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 255.13

Ref: 10-F015329