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55045-00-6

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55045-00-6 Usage

Heterocyclic compound

The molecule contains a ring structure with at least one atom not part of a carbon chain, in this case, nitrogen.

Indole class

The compound belongs to a class of chemical compounds that have a five-membered ring with a benzene ring attached to it.

Derivative of serotonin

The molecule is structurally similar to the neurotransmitter serotonin and acts as an agonist at certain serotonin receptors.

Antidepressant and anxiolytic properties

Tryptoline has been found to exhibit antidepressant (mood-brightening) and anxiolytic (anxiety-reducing) effects in animal models.

Potential treatment for sleep disorders

Tryptoline has been investigated for its potential role in modulating the sleep-wake cycle and has been proposed as a potential treatment for sleep disorders.

Further research needed

More research is needed to fully understand the pharmacological effects and potential therapeutic uses of tryptoline.

Check Digit Verification of cas no

The CAS Registry Mumber 55045-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,4 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55045-00:
(7*5)+(6*5)+(5*0)+(4*4)+(3*5)+(2*0)+(1*0)=96
96 % 10 = 6
So 55045-00-6 is a valid CAS Registry Number.

55045-00-6Downstream Products

55045-00-6Relevant articles and documents

Synthesis of 2,6,7-Trisubstituted Prenylated indole

Shiozawa, Motoki,Iida, Keisuke,Odagi, Minami,Yamanaka, Masahiro,Nagasawa, Kazuo

, p. 7276 - 7280 (2018/07/15)

Prenylated indole alkaloids bearing more than one prenyl or reverse-prenyl group show various biological activities. Among them, synthesis of trisubstituted-type prenylated indoles have not been well explored because of the difficulty in regioselective introduction of multiple prenyl and reverse-prenyl groups due to steric hindrance problems. Herein, we describe a synthesis of 2,6,7-trisubstituted prenylated indole using aza-Claisen rearrangement under mild conditions to introduce a prenyl group at C7 in the presence of the prenyl group at C6.

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