161511-86-0 Usage
Structure
It is an ester formed between 2-Azabicyclo[2.2.1]heptane-3-carboxylicacid and ethyl alcohol, with a specific stereochemistry denoted by the (1R,3R,4S) designation.
Application
Commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds.
Importance
Its unique molecular structure and stereochemistry make it a valuable building block in organic chemistry and drug development.
Safety
Requires careful handling and adherence to safety regulations due to potential hazards and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 161511-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,5,1 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161511-86:
(8*1)+(7*6)+(6*1)+(5*5)+(4*1)+(3*1)+(2*8)+(1*6)=110
110 % 10 = 0
So 161511-86-0 is a valid CAS Registry Number.
161511-86-0Relevant articles and documents
HETEROCYCLIC ETHER AND THIOETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION
-
Page 16, (2010/02/05)
Novel compounds having formulas (I), (II) or (III) or pharmaceutically-acceptable salts or prodrugs thereof, which are useful for controlling synaptic transmission; to therapeutically-effective pharmaceutical compositions of these compounds; and to the us
Bridged bicyclic vasopressin receptor antagonists with V2-selective or dual V1a/V2 activity
Dyatkin, Alexey B.,Hoekstra, William J.,Hlasta, Dennis J.,Andrade-Gordon, Patricia,De Garavilla, Lawrence,Demarest, Keith T.,Gunnet, Joseph W.,Hageman, William,Look, Richard,Maryanoff, Bruce E.
, p. 3081 - 3084 (2007/10/03)
The synthesis and biological testing of a novel series of nonpeptide vasopressin receptor antagonists, containing a bridged bicyclic nucleus, are reported. Variation of substituents (R1-R3) in general formula 3, and the configuration
