CAS 50877-41-3

1-benzyl-4-bromo-1H-pyrazole

Description:

1-Benzyl-4-bromo-1H-pyrazole is an organic compound characterized by its pyrazole ring, which is a five-membered aromatic heterocycle containing two nitrogen atoms. The presence of a benzyl group at the 1-position and a bromine atom at the 4-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents, reflecting its hydrophobic benzyl moiety. It may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the reactivity of the bromine atom. The pyrazole ring can also engage in hydrogen bonding, influencing its interactions in biological systems. 1-Benzyl-4-bromo-1H-pyrazole has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as pyrazole derivatives are known for their diverse biological activities. Safety data should be consulted for handling and usage, as halogenated compounds can pose health risks. Overall, this compound represents a valuable structure in organic synthesis and drug discovery.

Formula: C₁₀H₉BrN₂

InChI: InChI=1/C10H9BrN2/c11-10-6-12-13(8-10)7-9-4-2-1-3-5-9/h1-6,8H,7H2

SMILES: c1ccc(cc1)Cn1cc(cn1)Br

1-Benzyl-4-bromo-1H-pyrazole

CAS: 50877-41-3

Formula: C₁₀H₉BrN₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 237.0959

Ref: IN-DA00DACS

1-Benzyl-4-bromo-1H-pyrazole

CAS: 50877-41-3

1-Benzyl-4-bromo-1H-pyrazole

Formula: C₁₀H₉BrN₂

Purity: ≥95%

Color and Shape: off-white solid

Molecular weight: 237.10g/mol

Ref: 54-OR59333

1-Benzyl-4-bromopyrazole

CAS: 50877-41-3

Formula: C₁₀H₉BrN₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 237.1

Ref: 10-F048281

4-Bromo-1-(phenylmethyl)--1H-pyrazole

Controlled Product

CAS: 50877-41-3

Formula: C₁₀H₉BrN₂

Color and Shape: Neat

Molecular weight: 237.096

Ref: TR-B687070

1-Benzyl-4-bromo-1H-pyrazole

CAS: 50877-41-3

1-Benzyl-4-bromo-1H-pyrazole is a pyrazole derivative that can be synthesized from 1,2,3-triazoles and bromine. It undergoes arylation reactions in the presence of copper to form aryl derivatives. It is also catalytic mediated with alkyl halides to form c–h bond cleavage products. This compound reacts with tribromide to form an alkylation product. The ligand is activated by arylations and alkylations. It is used as a reagent in organic chemistry for the synthesis of pyrazole derivatives.

Formula: C₁₀H₉BrN₂

Purity: Min. 95%

Molecular weight: 237.1 g/mol

Ref: 3D-FB117271