structure of 6-(Acetoxymethyl)-3-aminotetrahydro-2h-pyran-2,4,5-triyl triacetate hydrochloride

6-(Acetoxymethyl)-3-aminotetrahydro-2h-pyran-2,4,5-triyl triacetate hydrochloride

CAS No.: 10034-20-5
M. Wt: 383.779
M. Fa: C14H22ClNO9
InChI Key: BQLUYAHMYOLHBX-XAWYEFCRSA-N
Appearance: White Solid

Names and Identifiers of 10034-20-5

CAS Number

10034-20-5

MDL Number

MFCD01075204

IUPAC Name

[(2R,3S,4R,5R,6S)-3,4,6-triacetyloxy-5-aminooxan-2-yl]methyl acetate;hydrochloride

InChI

InChI=1S/C14H21NO9.ClH/c1-6(16)20-5-10-12(21-7(2)17)13(22-8(3)18)11(15)14(24-10)23-9(4)19;/h10-14H,5,15H2,1-4H3;1H/t10-,11-,12-,13-,14-;/m1./s1

InChIKey

BQLUYAHMYOLHBX-XAWYEFCRSA-N

Canonical SMILES

CC(=O)OCC1C(C(C(C(O1)OC(=O)C)N)OC(=O)C)OC(=O)C.Cl

Isomeric SMILES

CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)OC(=O)C)N)OC(=O)C)OC(=O)C.Cl

UNSPSC Code

12352100

Physical and chemical properties of 10034-20-5

Boiling Point

429.5ºC at 760mmHg

Exact Mass

383.098297

Flash Point

158.3ºC

LogP

0.53050

Melting Point

197-200ºC

Molecular Formula

C14H22ClNO9

Molecular Weight

383.779

optical activity

[α]/D 30.0±2.0°, c = 1 in H2O

PSA

140.45000

RTECS

LZ6574000

Solubility

Methanol (Slightly), Water (Slightly)

Storage condition

Inert atmosphere,2-8°C

Vapour Pressure

1.39E-07mmHg at 25°C

Water Solubility

Soluble in water at 10mg/ml

Safety Information of 10034-20-5

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Interaction Studies of 10034-20-5

Research indicates that beta-Glucosamine, tetraacetate, hydrochloride interacts with various biological systems. Its interaction with cellular membranes has been studied for potential metabolic inhibition effects on glycoconjugates. These interactions are crucial for understanding its therapeutic potential and mechanisms of action within biological systems.

Biological Activity of 10034-20-5

This compound exhibits significant biological activity, particularly in the context of joint health. It primarily targets articular tissues such as cartilage and synovial membranes. The mechanism of action involves enhancing the synthesis of glycosaminoglycans, essential components of cartilage, which helps in retarding cartilage degradation and improving joint function. Additionally, beta-Glucosamine, tetraacetate, hydrochloride has been shown to reduce inflammation and enhance cellular redox status, making it a candidate for therapeutic interventions in inflammatory conditions.

Physical sample testing spectrum (NMR) of 10034-20-5

Physical sample testing spectrum (NMR) of 10034-20-5

Retrosynthesis analysis of 10034-20-5

  • Route#1

    Cas:3006-60-8
    Cas:10034-20-5
  • Route#2

    Cas:3068-34-6
    Cas:10034-20-5