199167-65-2 Usage
Cyclopentane derivative
It is derived from cyclopentane, a five-membered ring structure with a single bond between the carbon atoms.
Class
Cyclopentanols
It belongs to a group of organic compounds that contain a cyclopentane ring and one or more hydroxyl (-OH) groups.
Stereocenters
Positions 1, 3, 4, and 5
The compound has four chiral centers, which means it can exist in various stereoisomeric forms.
Configuration
(1S,3R,4R,5R)
The stereochemistry of the compound is defined by the (1S,3R,4R,5R) configuration, which describes the spatial arrangement of the atoms around the stereocenters.
Amino group
-NH2
The presence of an amino group makes the compound a potential candidate for various biological and pharmaceutical applications.
Hydroxymethyl group
-CH2OH
The hydroxymethyl group adds additional functionality to the molecule, which may contribute to its biological activity.
Biological activity
Potential pharmaceutical and biological applications
The compound's structure, including the amino and hydroxymethyl groups, suggests that it may have biological activity and could be used in the development of pharmaceuticals or other biological applications.
Research status
Further research needed
More research is required to fully understand the compound's properties, potential applications, and mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 199167-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,1,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 199167-65:
(8*1)+(7*9)+(6*9)+(5*1)+(4*6)+(3*7)+(2*6)+(1*5)=192
192 % 10 = 2
So 199167-65-2 is a valid CAS Registry Number.
199167-65-2Relevant articles and documents
Synthesis of isoaristeromycin from D-glucose
Singha,Tripathi,Roy,Achari,Mandal
, p. 919 - 924 (2007/10/03)
Isoaristeromycin 1, an analogue of the nucleoside antibiotic aristeromycin, has been synthesized by the application of intermolecular nitrone cycloaddition (INC) reaction on a D-glucose derived substrate.