115431-24-8

Basic information

• Product Name: HEPTYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
• Synonyms: HEPTYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE;Heptyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside;HEPTYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-SS-D-GLUCOPYRANOSIDE;Heptyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside
• CAS NO: 115431-24-8
• Molecular Formula: C21H35NO9
• Molecular Weight: 445.5039
• EINECS: 1533716-785-6
• Mol File: 115431-24-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 565.963 °C at 760 mmHg
• Flash Point: 296.084 °C
• Appearance: /
• Density: 1.162 g/cm³
• CAS DataBase Reference: HEPTYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: HEPTYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE(115431-24-8)
• EPA Substance Registry System: HEPTYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE(115431-24-8)

Safety Data

• Hazardous Substances Data: 115431-24-8(Hazardous Substances Data)

Usage

General Description

HEPTYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is a chemical compound that belongs to the group of glycosides. It is composed of a heptyl group attached to a glucopyranoside molecule, with multiple acetyl and acetamido groups attached to various positions on the glucopyranoside ring. HEPTYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE has potential applications in pharmaceutical and biomedical research, as it may exhibit bioactive properties due to its complex structure. Additionally, the heptyl group may confer lipophilic properties that could be useful in drug delivery systems. Further research is needed to fully understand the potential uses and effects of HEPTYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE.

Upstream product

• 111-70-6 n-heptan1ol 
• 10378-06-0 2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline 
• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 
• 170590-84-8 O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-N-hydroxysuccinimide 
• 1454311-01-3 1-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyloxy)benzotriazole 

Downstream Products

• 115414-54-5 O-(heptyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosid-3-yl)-D-lactoyl-L-alanyl-D-isoglutamine γ-benzyl ester 
• 115414-57-8 O-(heptyl 2-acetamido-2-deoxy-β-D-glucopyranosid-3-yl)-D-lactoyl-L-alanyl-D-isoglutamine γ-benzyl ester 
• 115414-52-3 heptyl 2-acetamido-4,6-O-benzylidene-3-O-(D-1-carboxyethyl)-2-deoxy-β-D-glucopyranoside 
• 115414-50-1 heptyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 115414-48-7 heptyl 2-acetamido-2-deoxy-β-D-glucopyranoside 

Relevant articles and documents

Glycosylated derivatives of substituted hydroxylamine. II. the phase transfer synthesis and the study of the glycosyl transfer reaction of glucosaminides of substituted hydroxylamine

The interaction of 1-(2-acetamido-3,4,6,-tri-O-acetyl-2-deoxy-β-D- glucopyranosyloxy)benzotriazole with primary and secondary aliphatic and cycloaliphatic alcohols or diisopropylidenegalactose in refluxing methylene chloride under the catalysis of Lewis a

SYNTHESIS OF GLYCOSIDIC ANALOGUES OF N-ACETYLNEURAMOYL-L-ALANYL-D-ISOGLUTAMINE

β-Heptyl and β-hexadecyl glycosides of N-acetylglucosamine have been obtained by the oxazoline method followed by deacetylation.Via a benzylidenation stage, the glycosides have been converted into the corresponding N-acetylmuramic acid derivatives and fro