21500-98-1 Usage
Description
Tenocyclidine, also known as TCP, is a tertiary amino compound consisting of a cyclohexane with piperidin-1-yl and thiophen-2-yl groups attached at position 1. It is a dissociative anesthetic drug with hallucinogenic and stimulant effects, similar to those of phencyclidine (PCP), but with a higher potency.
Uses
Used in Pharmaceutical Industry:
Tenocyclidine is used as a dissociative anesthetic for its ability to induce a state of anesthesia with hallucinogenic and stimulant effects. It is particularly useful in situations where traditional anesthetics may not be effective or when a more potent alternative is required.
Used in Research and Development:
Tenocyclidine is used as a research compound to study the effects of dissociative anesthetics on the central nervous system. Its potent hallucinogenic and stimulant properties make it a valuable tool for understanding the mechanisms behind these effects and potentially developing new treatments for various conditions.
Used in Veterinary Medicine:
In veterinary medicine, Tenocyclidine may be used as an anesthetic agent for animals, particularly in cases where a potent dissociative anesthetic is needed. Its effects on the central nervous system can be beneficial in managing pain and providing a stable anesthetic state during surgical procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 21500-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,0 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21500-98:
(7*2)+(6*1)+(5*5)+(4*0)+(3*0)+(2*9)+(1*8)=71
71 % 10 = 1
So 21500-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H23NS/c1-3-9-15(10-4-1,14-8-7-13-17-14)16-11-5-2-6-12-16/h7-8,13H,1-6,9-12H2
21500-98-1Relevant articles and documents
Preparation of tertiary alkyl carbinamines, propargylamines, and α-heteroarylamines by ketone-based aminoalkylation
Katritzky, Alan R.,Yang, Hongfang,Singh, Sandeep K.
, p. 286 - 290 (2007/10/03)
(Chemical Equation Presented). Ketones 6a-i were converted into their benzotriazolylamine adducts 8a-i either directly from the corresponding ketone 6a or via enamines 7b-i. Adducts 8a-i on treatment with Grignard reagents, lithium phenylacetylide, or heteroaryllithiums gave tertiary alkyl carbinamines 9a-h (47-61%), propargylamines 10a-i (30-98%), and α-heteroarylamines 11a-k (44-85%), respectively.
Carbon-13 nuclear magnetic resonance spectra of phenycyclidine analogs
Brine,Williams,Boldt,Carroll
, p. 1425 - 1429 (2007/10/05)
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