3814-34-4

Usage

Uses

1. Used in the Synthesis of Biologically Active Molecules:
1-Bromo-2-ethylbutane is used as a synthetic intermediate for the production of biologically active molecules. Its unique structure allows for the creation of a wide range of compounds with potential applications in the pharmaceutical and chemical industries.
2. Used in the Preparation of Dialkoxytriarylamine:
In the chemical industry, 1-Bromo-2-ethylbutane is utilized in the preparation of dialkoxytriarylamine, a type of organic compound with potential applications in various fields, including materials science and electronics.
3. Used as a Cysteine-Modifying Reagent:
1-Bromo-2-ethylbutane also serves as a cysteine-modifying reagent in the field of biochemistry. It is used to selectively modify the thiol group of cysteine residues in proteins, which can be crucial for studying protein structure, function, and interactions.

InChI:InChI=1/C6H13Br/c1-3-6(4-2)5-7/h6H,3-5H2,1-2H3

Upstream product

• 97-95-0 2-ethyl-1-butanol 

Downstream Products

• 5631-83-4 1-cyano-2-ethylbutane 
• 760-21-4 2-ethyl-1-butene 
• 617-79-8 2-ethyl-N-butylamine 
• 381209-09-2 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid 
• 239797-56-9 [4-(2-ethylbutoxy)phenylsulfanyl]acetic acid ethyl ester 
• 211515-46-7 1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride 
• 211513-21-2 Dalcetrapib 
• 211513-37-0 dalcetrapib 
• 211513-15-4 bis-[2-[1-(2-ethylbutyl)cyclohexanecarbonylamino]phenyl]disulfide 
• 34293-77-1 C₂₂H₂₂N₂O₇S₂^(2-)*2Na⁽¹⁺⁾ 
• 481630-90-4 5-bromo-1-(2-ethylbutyl)-1H-indole 
• 68506-84-3 (2-ethylbutyl)magnesium bromide 

Relevant academic research and scientific papers

Convergent synthesis of S-8921, a new potent hypocholesterolemic arylnaphthalene lignan analog

We established a convergent synthesis of S-8921 (1), a unique hypocholesterolemic lignan analog, in 9 steps, including concise preparations of phthalide 7 and acylpropenoate 10, and their regio- and stereocontrolled tandem anionic reactions leading to precursor 11 as a key step.

Scavenger assisted combinatorial process for preparing libraries of tertiary amine compounds

This invention relates to a novel solution phase process for the preparation of tertiary amine combinatorial libraries. These libraries have utility for drug discovery and are used to form wellplate components of novel assay kits.

Pheromones, 89.- Wittig Syntheses of Alkyl-Branched and Cyclic Analogs of (Z)-5-Decenyl Acetate, the Sex Pheromone of Agrotis segetum (Lepitoptera: Noctuidae)

By means of (Z)-selective Wittig olefination alkyl-branched and cyclic analogs of (Z)-5-decenyl acetate, the sex pheromone of the turnip moth, Agrotis segetum (Lepidoptera: Noctuidae), have been synthesized. Key Words: Pheromones / (Z)-5-decenyl acetate / Wittig reactions / Agrotis segetum

Synthesis and antiallergy activity of [1,3,4]thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d]pyrimidin-9(3H)-one derivatives. II. 6-Alkyl- and 6-cycloalkylalkyl derivatives

A series of 6-alkyl- or 6-(cycloalkylalkyl)-[1,3,4]thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d]pyr imidin-9(3H)-ones 1b-o was synthesized from the corresponding 1,3,4-thiadiazol-5-amines 3b-o and the antiallergic activities of the products were evaluated. Among the compounds 6-(2-cyclohexylethyl)-[1,3,4]thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d]p yrimidin-9(3H)-one 1h, whose X-ray crystallographic stereostructure is shown, was found to be a promising new antiallergic agent, which has low toxicity and dual activity as a leukotriene D4 receptor antagonist and as an orally active mast cell stabilizer.