3814-34-4 Usage
Description
1-Bromo-2-ethylbutane, also known as 2-ethylbutyl bromide, is an organic compound with the chemical formula C6H13Br. It is a clear colorless to light yellow liquid at room temperature and is commonly used as an intermediate in the synthesis of various organic compounds.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 3814-34-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,1 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3814-34:
(6*3)+(5*8)+(4*1)+(3*4)+(2*3)+(1*4)=84
84 % 10 = 4
So 3814-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H13Br/c1-3-6(4-2)5-7/h6H,3-5H2,1-2H3
3814-34-4Relevant articles and documents
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Rhinesmith
, p. 596,597 (1936)
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Scavenger assisted combinatorial process for preparing libraries of tertiary amine compounds
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, (2008/06/13)
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.
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
Yokohama,Miwa,Aibara,Fujiwara,Matsumoto,Nakayama,Iwamoto,Mori,Moroi,Tsukada,Isoda
, p. 2391 - 2398 (2007/10/02)
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.