115414-47-6 Usage
Description
HEXADECYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is a glycoside chemical compound that consists of a 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-beta-D-glucopyranoside molecule with a hexadecyl group attached to it. HEXADECYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is widely used in scientific research, particularly in the field of carbohydrate chemistry and biochemistry, as well as in pharmaceutical development and drug formulation. Its unique properties and applications make it a significant compound in various scientific and industrial processes.
Uses
Used in Carbohydrate Chemistry Research:
HEXADECYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a research compound in carbohydrate chemistry for studying the structure, properties, and reactions of carbohydrates and their derivatives. Its unique structure allows researchers to investigate various aspects of carbohydrate chemistry, such as glycosidic bond formation, carbohydrate recognition, and carbohydrate-based drug design.
Used in Biochemistry Research:
In biochemistry, HEXADECYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a research tool to study the interactions between carbohydrates and proteins, enzymes, and other biomolecules. Its specific properties enable researchers to explore the role of carbohydrates in biological processes, such as cell signaling, immune response, and molecular recognition.
Used in Pharmaceutical Development:
HEXADECYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is utilized in pharmaceutical development as a potential drug candidate or as a building block for the synthesis of carbohydrate-based drugs. Its unique structure and properties make it a promising compound for the development of new therapeutic agents, particularly in the treatment of various diseases and disorders.
Used in Drug Formulation:
In drug formulation, HEXADECYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as an excipient or an active pharmaceutical ingredient (API) to improve the solubility, stability, and bioavailability of drug formulations. Its specific properties allow it to enhance the performance of drug formulations, leading to more effective and safer medications.
Used in Chemical Synthesis:
HEXADECYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is employed in chemical synthesis as a starting material or an intermediate for the synthesis of various complex organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactivity make it a valuable compound for the development of new synthetic routes and methods.
Used in Material Science:
In material science, HEXADECYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a component in the development of advanced materials, such as polymers, coatings, and sensors. Its specific properties, such as its ability to form hydrogen bonds and its compatibility with other materials, make it a promising candidate for the creation of innovative materials with unique properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 115414-47-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,4,1 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 115414-47:
(8*1)+(7*1)+(6*5)+(5*4)+(4*1)+(3*4)+(2*4)+(1*7)=96
96 % 10 = 6
So 115414-47-6 is a valid CAS Registry Number.
115414-47-6Relevant articles and documents
Synthesis of β-glycosides of N-acetylglucosamine in the presence of HgI2
Zemlyakov,Kur'yanov,Chirva
, p. 352 - 355 (1996)
The use of HgI2 as catalyst in the synthesis of trans-glycosides of N-acetylglucosamine is described. Using this catalyst, β-glycosides of N-acetylglucosamine with aglycons of different structures and lyophilicities have been synthesized. The p
Synthesis of oligosaccharides designed to form micelles, corresponding to structures found in ovarian cyst fluid
Buskas, Therese,Konradsson, Peter
, p. 25 - 51 (2007/10/03)
The syntheses of α-D-GlcpNAc-(1 →4)-β-D-Galp-(1→4)-β-D-GlcNAc-(1→O)-(CH2)15CH3 (1) and fragments thereof, corresponding to structures found in human ovarian cyst fluid, are described. Silver triflate promoted coupling of 3.4,6-tri-O-acetyl-2-azido-2-deoxy-β-D-glucopyranosyl bromide (12) and galactose acceptor (11) gave a disaccharide donor (13), which was readily transformed into the corresponding bromoderivative 18. For the synthesis of disaccharide β-D-Galp-(1 →4)-D-GlcNAc, several differently protected glucosamine acceptors were prepared. It was found that cetyl alcohol needed to be introduced after the formation of the β-galactoside bond. Glycosylation of pent-4-enyl 3,6-di-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside (30) with (3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-(1 →4)-2,3,6-tri-O-benzoyl-α-D-galactopyranosyl bromide (18) by use of silver triflate as promoter gave the desired trisaccharide 31. Finally 31 was transformed via coupling to the long alkyl chain aglycon and deprotection into the title compound 1.
