76899-76-8 Usage
Molecular structure
A complex derivative of glucopyranoside with a methyl group (CH3) attached to the first carbon, a benzylidene group (C6H5-CH=) attached to the fourth and sixth carbons, and an amino (-NH2) and a hydroxy group (-OH) attached to the second carbon.
Chemical classification
A glucopyranoside derivative, which is a type of sugar molecule with a six-membered carbon ring and an oxygen atom at the first position.
Functional groups
Contains a methyl group, a benzylidene group, an amino group, and a hydroxy group, which contribute to its chemical reactivity and potential biological activities.
Stereochemistry
The compound has a β-D-glucopyranosid configuration, meaning the glucose ring is in a chair conformation and the hydroxy groups are positioned in an alternating axial and equatorial arrangement.
Biological activity
1-O-Methyl-2-amino-2-deoxy-4,6-O-benzyliden-β-D-glucopyranosid is known for its potential biological activities and therapeutic applications, making it a valuable compound in pharmaceutical research and drug development.
Applications
Commonly used in pharmaceutical research and drug development to study its potential role in various biological processes and to develop new therapeutic agents.
Context-dependent functions
The specific role and functions of 1-O-Methyl-2-amino-2-deoxy-4,6-O-benzyliden-β-D-glucopyranosid depend on the context and purpose for which it is being utilized, such as targeting specific diseases or biological pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 76899-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,9 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76899-76:
(7*7)+(6*6)+(5*8)+(4*9)+(3*9)+(2*7)+(1*6)=208
208 % 10 = 8
So 76899-76-8 is a valid CAS Registry Number.
76899-76-8Relevant articles and documents
Synthesis of glucosamine vinyl ether derivative and its deuterated analog
Ledovskaya, M. S.,Rodygin, K. S.,Voronin, V. V.
, p. 1401 - 1404 (2020/09/07)
The use of calcium carbide (in the presence of H2O) as a source of acetylene in the reaction with methyl 2-amino-4,6-O-benzylidene-2-deoxy-β-d-glucopyranoside under superbasic conditions (KF, KOH, DMSO, 130 °C, 3 h) led to the corresponding vin
Selective N-sulfation of glucosamine derivatives using phenyl chlorosulfate in non-aqueous solvent
Kerns, Robert J.,Linhardt, Robert J.
, p. 2671 - 2680 (2007/10/03)
The selective N-sulfation of 2-amino-2-deoxy-D-glucopyranose derivatives having unprotected hydroxyl groups with phenyl chlorosulfate and triethylamine in anhydrous organic solvent followed by addition of aqueous sodium bicarbonate affords high yields of
Metal Complexes with Biological Important Ligands, XXVII. Palladium(II) and Platinum(II) Complexes with Aminomonosaccharides
Thiel, Gerhard,Beck, Wolfgang
, p. 1081 - 1093 (2007/10/02)
A series of dihalo palladium and platinum complexes X2PtL2 (X = Cl, I) with aminosugars L = 2-amino-2-deoxy-1,3,4,6-tetra-O-acetyl-β-D-glucopyranose, 1-O-methyl-2-amino-2-deoxy-4,6-O-benzyliden-α,β-D-glucopyranoside, 1-O-methyl-2-amino-2-deoxy-α,β-D-glucopyranoside, 6-amino-6-deoxy-1,2:3,4-di-O-isopropyliden-α-D-galactopyranose has been prepared and characterized by their IR, 1H and 13C NMR spectra.Monosaccharides and aminomonosaccharides have been attached to the complex via the carboxygroup of α-amino acid PtII complexes to give esters or amides with the monosaccharides as the alcohol or amine components, respectively. - Key words: Aminomonosaccharides, Palladium(II) Complexes, Platinum(II) Complexes
