92527-13-4 Usage
Uses
Used in Organic Synthesis:
2-(BUT-1-YL)-TETRAHYDRO-4-H-1,3,6,2-DIOXAZABOROCINE is used as an intermediate in organic synthesis for the preparation of various functionalized compounds. Its unique molecular structure and reactivity make it a valuable building block for the development of new organic molecules.
Used in Material Science:
In the field of material science, 2-(BUT-1-YL)-TETRAHYDRO-4-H-1,3,6,2-DIOXAZABOROCINE is used for the development of new materials with special properties. Its boron-containing framework can contribute to the creation of materials with unique characteristics, making it a promising candidate for various applications.
Used in Biomedical Applications:
2-(BUT-1-YL)-TETRAHYDRO-4-H-1,3,6,2-DIOXAZABOROCINE is also of interest for potential use in biomedical applications. Its boron-containing framework may offer unique properties that can be harnessed for the development of new therapeutic agents or diagnostic tools.
Used as a Catalyst in Chemical Reactions:
Furthermore, 2-(BUT-1-YL)-TETRAHYDRO-4-H-1,3,6,2-DIOXAZABOROCINE can be used as a catalyst in various chemical reactions. Its unique reactivity and boron-containing framework can facilitate specific chemical transformations, making it a valuable asset in the development of new synthetic methods and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 92527-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,2 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92527-13:
(7*9)+(6*2)+(5*5)+(4*2)+(3*7)+(2*1)+(1*3)=134
134 % 10 = 4
So 92527-13-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H18BNO2/c1-2-3-4-9-11-7-5-10-6-8-12-9/h10H,2-8H2,1H3
92527-13-4Relevant academic research and scientific papers
TREATMENT OF OSTEOARTHRITIS PAIN
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Paragraph 0205, (2016/04/26)
This invention discloses a method of treatment of osteoarthritis pain by administration of a histamine H3 receptor antagonist, described herein, a salt thereof, or a composition comprising such compound or salt.
CYCLOPROPYL AMINE DERIVATIVES
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Page/Page column 75; 79-80, (2008/06/13)
Compounds of formula (I) are useful in treating conditions or disorders prevented by or ameliorated by histamine-3 receptor ligands. Also disclosed are pharmaceutical compositions comprising the histamine-3 receptor ligands, methods for using such compoun
Enantioselective cyclopropanation of allylic alcohols with dioxaborolane ligands: Scope and synthetic applications
Charette, André B.,Juteau, Hélène,Lebel, Hélène,Molinaro, Carmela
, p. 11943 - 11952 (2007/10/03)
A very effective chiral controller has been found for the conversion of allylic alcohols into the corresponding enantiomerically enriched cyclopropanes using bis(iodomethyl)zinc. A variety of chiral, nonracemic cyclopropylmethanols could be obtained according to this method. This methodology was extended with success to the cyclopropanation of unconjugated and conjugated polyenes and homoallylic alcohols. The cyclopropanation of allylic carbamates has also been investigated with this system, but it was found that enantioenriched cyclopropylmethylamines are best prepared from enantioenriched cyclopropylmethanols.
