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N-(3,4-dimethoxybenzyl)-N-(2-thienylmethyl)amine, also known as Tiletamine, is a dissociative anesthetic and an NMDA receptor antagonist with sedative and analgesic properties. It is used in veterinary medicine for inducing a state of dissociative anesthesia in various animal species.

502935-34-4

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502935-34-4 Usage

Uses

Used in Veterinary Medicine:
N-(3,4-dimethoxybenzyl)-N-(2-thienylmethyl)amine is used as an anesthetic agent for inducing dissociative anesthesia in animals, particularly in combination with zolazepam as a drug called Telazol. It is effective in producing sedation, analgesia, and unresponsiveness to external stimuli while maintaining cardiorespiratory function.
Used in Various Animal Species:
N-(3,4-dimethoxybenzyl)-N-(2-thienylmethyl)amine is used as an anesthetic for a wide range of animal species, including dogs, cats, and non-human primates, due to its wide safety margin and efficacy.
Controlled Substance:
N-(3,4-dimethoxybenzyl)-N-(2-thienylmethyl)amine is considered a controlled substance in some countries, and its use is restricted to licensed professionals in medical and veterinary settings to ensure safe and appropriate administration.

Check Digit Verification of cas no

The CAS Registry Mumber 502935-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,9,3 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 502935-34:
(8*5)+(7*0)+(6*2)+(5*9)+(4*3)+(3*5)+(2*3)+(1*4)=134
134 % 10 = 4
So 502935-34-4 is a valid CAS Registry Number.

502935-34-4Relevant academic research and scientific papers

A general and efficient PIFA mediated synthesis of heterocycle-fused quinolinone derivatives

Herrero, M.Teresa,Tellitu, Imanol,Domínguez, Esther,Hernández, Susana,Moreno, Isabel,SanMartín, Raúl

, p. 8581 - 8589 (2007/10/03)

A new application of the hypervalent iodine reagent phenyliodine(III)bis(trifluoroacetate) (PIFA) has been developed for the construction of a series of N, O, S-containing heterocycle-fused quinolinone derivatives in a general and efficient way. An altern

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