15648-16-5 Usage
Description
4-METHYL-MORPHOLINEBORANE is an organic compound that serves as a versatile reagent in various chemical and biochemical applications. It is known for its ability to facilitate specific reactions and analyses, making it a valuable tool in the field of chemistry.
Uses
Used in Chemical Analysis:
4-METHYL-MORPHOLINEBORANE is used as a reagent for the labeling of oligosaccharides, enabling their quantitative analysis through mass spectrometry. This application is crucial for the study of complex carbohydrates and their roles in biological systems.
Used in Microbiology:
In the field of microbiology, 4-METHYL-MORPHOLINEBORANE is utilized for the analysis of sugar markers associated with Bacillus anthracis spores after culture. This helps in the identification and characterization of these spores, which are significant in the study of anthrax and related diseases.
Used in Carbohydrate Chemistry:
4-METHYL-MORPHOLINEBORANE is employed in the synthesis of sulfated red seaweed galactan derived disaccharide alditol. This application is essential for the development of novel bioactive compounds with potential applications in various industries, including pharmaceuticals and biotechnology.
Used in Analytical Chemistry:
The compound is also used as a reactant for methanolic cleavage, which is a crucial step in the analysis of sulfated galactans from red algae. This process involves reductive hydrolysis and mild methanolysis, followed by high-performance liquid chromatography (HPLC) to separate and identify the resulting products.
Used in Polymer Science:
In the field of polymer science, 4-METHYL-MORPHOLINEBORANE is used in the reductive pyrolysis of carrageenan, a natural polysaccharide found in red seaweed. This process is carried out using high-performance anion-exchange chromatography, which allows for the detailed analysis of the resulting products and their potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 15648-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,4 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15648-16:
(7*1)+(6*5)+(5*6)+(4*4)+(3*8)+(2*1)+(1*6)=115
115 % 10 = 5
So 15648-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H13BNO/c1-7(6)2-4-8-5-3-7/h2-6H2,1H3
15648-16-5Relevant articles and documents
Crown-ether-catalysed synthesis of amine borane and amine trideuterioborane adducts from NaBH4-NaBD4 in ether
Kampel, V.,Warshawsky, A.
, p. 15 - 18 (2007/10/02)
Amine borane and amine trideuterioborane adducts have been obtained in good yield by the crown-ether-catalysed reaction of R3N*HCl with NaBH4 and NaBD4 in ether.The absence of isotopic exchange in the reaction with NaBD4 is demonstrated by IR and 11B and
Chemistry of boranes. XV. Synthesis of diborane from boric oxide
Ford,Kalb,Mcclelland,Muetterties
, p. 1032 - 1035 (2008/10/08)
A direct synthesis of diborane from boric oxide has been achieved by hydrogenation of the oxide in the presence of aluminum and aluminum trichloride. Very pure diborane is obtained from this reaction in 40-50% conversions at temperatures above 150° and hydrogen pressures of 750 atm. This hydrogenation is believed to proceed through an aluminum chlorohydride intermediate. Amine boranes, aminoboranes, and borazines were obtained directly from boric oxide when the hydrogenation was effected in the presence of secondary or tertiary alkylamines.
