Product Name:4-Bromo-N-isopropylbenzamide

IUPAC Name:4-bromo-N-(propan-2-yl)benzamide

CAS:336182-29-7
Molecular Formula:C10H12BrNO
Purity:95%
Catalog Number:CM192835
Molecular Weight:242.12

Packing Unit Available Stock Price($) Quantity
CM192835-10g 3-4 Weeks ȋŸŸ
CM192835-25g 3-4 Weeks œşş

For R&D use only.

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Product Details

CAS NO:336182-29-7
Molecular Formula:C10H12BrNO
Melting Point:-
Smiles Code:O=C(NC(C)C)C1=CC=C(Br)C=C1
Density:
Catalog Number:CM192835
Molecular Weight:242.12
Boiling Point:344.6°C at 760 mmHg
MDL No:MFCD00465197
Storage:Store at 2-8°C.

Category Infos

Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

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Product Other Information

Product Overview 4-Bromo-N-isopropylbenzamide (4-BIB) is an organic compound with a wide range of applications in biochemistry, pharmacology and other scientific fields. In biochemistry, 4-BIB is used as a reagent for the synthesis of various compounds, and its mechanism of action can be used to study the biochemical and physiological effects of drugs. In pharmacology, 4-BIB is used to study the effects of drug interactions on the body, and its advantages and limitations are useful in designing lab experiments.
Synthesis and Application 4-Bromo-N-isopropylbenzamide is synthesized through the reaction of 4-bromo-N-isopropylbenzamide with an acid such as hydrochloric acid. The reaction is catalyzed by a strong base such as potassium hydroxide and proceeds through a nucleophilic substitution mechanism. The reaction can be carried out in either an aqueous or organic medium, and the product can be isolated by crystallization. 4-Bromo-N-isopropylbenzamide has numerous scientific research applications, including drug development, drug-drug interactions, and biochemical and physiological studies. In drug development, 4-Bromo-N-isopropylbenzamide is used to study the effects of drug interactions on the body. In drug-drug interactions, 4-Bromo-N-isopropylbenzamide is used to study the effects of two drugs interacting with each other, and to determine the optimal dose of each drug. In biochemical and physiological studies, 4-Bromo-N-isopropylbenzamide is used to study the biochemical and physiological effects of drugs on the body.
Future Directions The potential future directions for 4-Bromo-N-isopropylbenzamide include its use in drug discovery, drug-drug interactions, and biochemical and physiological studies. Additionally, 4-Bromo-N-isopropylbenzamide could be used to study the effects of drugs on the body, and to develop more effective drugs with fewer side effects. Finally, 4-Bromo-N-isopropylbenzamide could be used to develop new drugs that target specific receptors, and to study the effects of drug-drug interactions on the body.