764667-66-5 Usage
Chemical structure
A complex chemical compound with a 1,3-dioxane ring and various substituents.
Derivative
It is a derivative of 1,3-dioxane, a heterocyclic compound.
Substituents
Contains a substituted hydroxy-ethylidene group and difluorophenyl groups.
Hydroxyethylidene group
Potentially allows the compound to interact with biological macromolecules.
Difluorophenyl groups
May contribute to the compound's stability and activity.
Dimethyl groups
Present in the compound, possibly enhancing its stability and activity.
Pharmaceutical or medicinal applications
Likely due to the presence of the hydroxyethylidene group.
Further research
Necessary to fully understand the compound's potential uses and effects.
Molecular weight
Approximately 214.15 g/mol (calculated from the molecular formula).
Check Digit Verification of cas no
The CAS Registry Mumber 764667-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,4,6,6 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 764667-66:
(8*7)+(7*6)+(6*4)+(5*6)+(4*6)+(3*7)+(2*6)+(1*6)=215
215 % 10 = 5
So 764667-66-5 is a valid CAS Registry Number.
764667-66-5Relevant articles and documents
Expanded Structure-Activity Studies of Lipoxazolidinone Antibiotics
Mills, Jonathan J.,Pierce, Joshua G.,Robinson, Kaylib R.
supporting information, p. 374 - 377 (2019/03/21)
The lipoxazolidinone family of marine natural products, which contains an unusual 4-oxazolidinone core, was found to possess potent antimicrobial activity against methicillin resistant Staphylococcus aureus (MRSA). Herein, we expanded our previous synthet
PROCESS AND INTERMEDIATES FOR THE PREPARATION OF BETA-AMINO ACID AMIDE DIPEPTIDYL PEPTIDASE-IV INHIBITORS
-
Page 15, (2010/02/08)
A novel process is provided for the preparation of chiral beta-amino acid amide inhibitors of the dipeptidyl peptidase-IV and the useful intermediates obtained therein. The products resulting from the instant process are inhibitors of dipeptidyl peptidase-IV and thereby useful for the treatment of Type 2 diabetes.
