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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.

21500-98-1

21500-98-1 Suppliers

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21500-98-1 Usage

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

21500-98-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tenocyclidine

1.2 Other means of identification

Product number -
Other names Tenociclidina [INN-Spanish]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21500-98-1 SDS

21500-98-1Downstream Products

21500-98-1Relevant academic research and scientific papers

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.

SUBSTITUTED 1-(2-THIENYL)CYCLOHEXYLAMINES AND RELATED COMPOUNDS AS POTENTIAL NMDA ANTAGONISTS

Sindelar, Karel,Dobrovsky, Karel,Krejci, Ivan,Polivka, Zdenek

, p. 894 - 902 (2007/10/02)

Reactions of bisulfite addition compounds prepared in situ from cyclohexanone or 3,4,5,6-tetrahydro-2H-thiopyran-3-one with potassium cyanide and corresponding amines resulted with high yields in amino nitriles type of V and VI.These compounds were subjected to reactions with 2-thienylmagnesium bromide and in the case of the amino nitriles Vc and Vf with 5-bromo-2-thienylmagnesium bromide.Only in the case of compound Vf, a by-product X was isolated in addition to the desired 1-piperidine (VIIf).Compound VIIf was used for the synthesis of the carboxylic acid XI.The compounds prepared were tested by some methods of biochemical and behavioural pharmacology.