190912-49-3

Basic information

• Product Name: HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
• Synonyms: HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE;Hexyl2-acetamido-2-deoxy-b-D-glucopyranoside;HEXYL 2-ACETAMIDO-2-DEOXY-SS-D-GLUCOPYRANOSIDE;Hexyl 2-acetamido-2-deoxy-β-D-glucopyranoside;HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSID
• CAS NO: 190912-49-3
• Molecular Formula: C14H27NO6
• Molecular Weight: 305.36728
• EINECS: 1533716-785-6
• Mol File: 190912-49-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE(190912-49-3)
• EPA Substance Registry System: HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE(190912-49-3)

Safety Data

• Hazardous Substances Data: 190912-49-3(Hazardous Substances Data)

Usage

General Description

HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is a chemical compound that belongs to the family of glycosides. It is a derivative of glucose and has a hexyl group attached to the sugar molecule. HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is commonly used in the field of pharmaceuticals and biochemistry for various purposes such as drug delivery and synthesis of glycoconjugates. It has also been studied for its potential antibacterial and antiviral properties, as well as its role in cancer therapy. Additionally, it is used in cosmetic formulations and skincare products for its moisturizing and emulsifying properties. Overall, HEXYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE has a wide range of applications in different industries due to its unique chemical structure and diverse properties.

Upstream product

• 111-27-3 hexan-1-ol 
• 172945-26-5 1-hexyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 
• 10378-06-0 2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline 

Downstream Products

• 231607-07-1 1-hexyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 172945-30-1 Hexyl 2-acetamido-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 172945-32-3 Hexyl 2-acetamido-6-O-benzyl-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-2-deoxy-β-D-glucopyranoside 
• 172945-34-5 Hexyl 2-acetamido-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-6-O-benzyl-2-deoxy-4-O-<3-<(methyl 4,7,8,9-tetra-O-acetyl-N-acetyl-α-D-neuraminate-2-yl)oxy>propoxymethyl>-β-D-glucopyranoside 
• 231607-27-5 1-hexyl 2-acetamido-4,6-O-benzylidene-3-O-<2-(4-<4-phenyl>butanamido)ethyl>-2-deoxy-β-D-glucopyranoside 
• 231607-09-3 1-hexyl 2-acetamido-4,6-O-benzylidene-3-O-(4-<4-phenyl>butanoyl)-2-deoxy-β-D-glucopyranoside 
• 231607-16-2 1-hexyl 4,6-O-benzylidene-2-(4-<4-phenyl>butanamido)-2-deoxy-β-D-glucopyranoside 
• 231607-26-4 1-hexyl 2-acetamido-4,6-O-benzylidene-3-O-cyanomethyl-2-deoxy-β-D-glucopyranoside 
• 231607-08-2 1-hexyl 2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 500767-94-2 (R)-4-{(S)-2-[(R)-2-((2R,3R,4R,5S,6R)-3-Acetylamino-2-hexyloxy-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-4-yloxy)-propionylamino]-propionylamino}-4-carbamoyl-butyric acid benzyl ester 
• 172945-27-6 Hexyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 

Relevant articles and documents

N-Acetylmuramyl-L-Alanyl-D-Isoglutamine Glycosides: Effect of Glycoside Bond Configuration and Aglycone on Biological Activity

Hexyl, octyl, and cyclohexyl β-glycosides and heptyl and cyclohexyl α-glycosides of muramyl dipeptide (MDP) were synthesized. Tests in vitro and in vivo revealed lower immunostimulating activities of MDP α-glycosides in comparison with the corresponding β-glycosides and MDP itself. In the case of alkyl β-glycosides, differences in hydrocarbon chain lengths (C4-C8) and in aglycone (aliphatic chain and aliphatic or aromatic ring) exerted no substantial effect on the immunostimulating activity.

Alkylating agents from sugars. Alkyl hexopyranoside derivatives as carrier systems for chlorambucil

Chlorambucil derivatives involving alkyl 2-aminodeoxy sugars have been synthesized in good yield by coupling the chlorambucil moiety to positions C-2 or C-3 of the sugar, directly or via a spacer. The starting material was easily available from 2-acetamido-2-deoxy-D-glucose. The final compounds were tested for cytotoxicity, and some of those that presented the best results were studied for inhibition of cell proliferation. Copyright (C) 1999 Elsevier Science Ltd.