CAS 155054-42-5

4-IPAB

Description:

4-IPAB, or 4-Iodo-2-(pyridin-4-yl)aniline, is a chemical compound characterized by its iodo-substituted aromatic structure, which includes a pyridine ring. This compound typically exhibits properties associated with both aromatic amines and halogenated compounds, such as moderate solubility in organic solvents and potential reactivity due to the presence of the iodine atom. The iodo group can enhance the compound's electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the pyridine moiety may contribute to its biological activity, as many pyridine derivatives are known for their pharmacological properties. 4-IPAB is often utilized in organic synthesis and may serve as an intermediate in the production of more complex molecules. Safety considerations should be taken into account due to the potential toxicity of aromatic amines and halogenated compounds. Overall, 4-IPAB is a versatile compound with applications in both research and industrial settings.

Formula: C₁₄H₁₉IN₂O

InChI: InChI=1/C14H19IN2O/c15-13-6-4-12(5-7-13)14(18)16-8-11-17-9-2-1-3-10-17/h4-7H,1-3,8-11H2,(H,16,18)

SMILES: C1CCN(CC1)CCNC(=O)c1ccc(cc1)I

Synonyms:

• 4-iodo-N-piperidinoethylbenzamide
• 4-iodo-N-[2-(piperidin-1-yl)ethyl]benzamide

4-iodo-N-[2-(piperidin-1-yl)ethyl]benzamide

CAS: 155054-42-5

Formula: C₁₄H₁₉IN₂O

Purity: 98%

Molecular weight: 358.2179

Ref: IN-DA001NKP

4-Iodo-N-[2-(1-piperidinyl)ethyl]benzamide

CAS: 155054-42-5

4-Iodo-N-[2-(1-piperidinyl)ethyl]benzamide

Purity: ≥95%

Molecular weight: 358.22g/mol

Ref: 54-OR89526

4-Iodo-N-[2-(1-piperidinyl)ethyl]benzamide

CAS: 155054-42-5

Purity: 98%

Molecular weight: 358.2229919

Ref: 10-F601198

N-[2-(Piperidinylamino)ethyl]-4-iodobenzamide

CAS: 155054-42-5

2-(Piperidinylamino)ethan-1-amine hydrochloride is a potent immunomodulator. It inhibits bacterial translocation from the intestine to the mesenteric lymph nodes and reduces the number of inflammatory cells in the intestine. 2-(Piperidinylamino)ethan-1-amine hydrochloride has also been shown to reduce bacterial translocation in mice with infectious colitis, which is caused by Shigella flexneri or Salmonella typhimurium. 2-(Piperidinylamino)ethan-1-amine hydrochloride binds to bacterial DNA gyrase and inhibits bacterial replication by inhibiting dna synthesis, protein synthesis, and cell division. This drug also binds to an effector protein, which may play a role in its immunomodulatory activities.

Formula: C₁₄H₁₉IN₂O

Purity: Min. 95%

Molecular weight: 358.22 g/mol

Ref: 3D-FGA05442