131556-11-1 Usage
Uses
Used in Chemical Synthesis:
8a-phenyldecahydroquinoline is used as an intermediate compound for the synthesis of other organic substances. Its unique structure allows it to participate in various chemical reactions, making it a valuable component in the creation of new compounds.
Used in Pharmaceutical Research:
8a-phenyldecahydroquinoline is used as a potential candidate in pharmaceutical research for the development of new drugs. Its chemical properties and reactivity may contribute to the discovery of novel therapeutic agents.
Used in Material Science:
8a-phenyldecahydroquinoline is used as a component in the development of new materials. Its structural characteristics could be exploited to create materials with unique properties for various applications in different industries.
Used in Analytical Chemistry:
8a-phenyldecahydroquinoline is used as a reference compound or a standard in analytical chemistry for the identification and quantification of similar compounds. Its distinct chemical properties can aid in the development of analytical methods and techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 131556-11-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,5,5 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131556-11:
(8*1)+(7*3)+(6*1)+(5*5)+(4*5)+(3*6)+(2*1)+(1*1)=101
101 % 10 = 1
So 131556-11-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H21N/c1-2-7-13(8-3-1)15-11-5-4-9-14(15)10-6-12-16-15/h1-3,7-8,14,16H,4-6,9-12H2
131556-11-1Relevant articles and documents
Synthesis and biological activity of 8a-phenyldecahydroquinolines as probes of PCP's binding conformation. A new PCP-like compound with increased in vivo potency
Chen,Kozikowski,Wood,Reynolds,Ball,Pang
, p. 1634 - 1638 (2007/10/02)
The synthesis and chemical resolution of cis- and trans-fused 8a- phenyldecahydroquinolines 3 and 4 are described together with the affinity of the four optically pure compounds for the PCP recognition site of the NMDA receptor complex. These compounds we
AN UNUSUAL FRAGMENTATION PROCESS DISCOVERED DURING THE COURSE OF CLEAVAGE OF A CAMPHANIC ACID AMIDE
Kozikowski, Alan P.,Chen, Chinpiao,Ball, Richard G.
, p. 5869 - 5872 (2007/10/02)
An unusual fragmentation reaction that affords a carbamoyl anion discovered during the course of the synthesis of rigidified PCP analogues is reported.
