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3-Benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione, also known as bemitil, is a synthetic heterocyclic compound with a bicyclic diazabicyclooctane ring system. It has been identified as an actoprotector and adaptogen, exhibiting neuroprotective, anti-fatigue, and anti-stress properties. Bemitil has potential applications in the treatment of neurological disorders, mental fatigue, and cognitive function enhancement.

17783-46-9

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17783-46-9 Usage

Uses

Used in Pharmaceutical Industry:
Bemitil is used as a therapeutic agent for neurological disorders and mental fatigue due to its neuroprotective, anti-fatigue, and anti-stress properties.
Used in Cognitive Function Enhancement:
Bemitil is used as a cognitive enhancer to improve memory and cognitive function, making it a promising compound for the development of therapeutic agents for neurological and mental health conditions.
Used in Physical Performance Improvement:
Bemitil is used as a performance enhancer to improve physical performance, enhance endurance, and increase tolerance to stress.

Check Digit Verification of cas no

The CAS Registry Mumber 17783-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,8 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17783-46:
(7*1)+(6*7)+(5*7)+(4*8)+(3*3)+(2*4)+(1*6)=139
139 % 10 = 9
So 17783-46-9 is a valid CAS Registry Number.

17783-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-Benzyl-8-methyl-3,8-diazabicyclo<3.2.1>octan-2,4-dion

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:17783-46-9 SDS

17783-46-9Relevant academic research and scientific papers

NOVEL 3,8-DIAZA-BICYCLO[3.2.1]OCTANE- AND 3,9-DIAZA-BICYCLO[3.3.1]-NONANE-3-CARBOXYLIC ACID ESTER DERIVATIVES AND THEIR USE AS MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITORS

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Page/Page column 18, (2009/10/22)

This invention relates to novel 3,8-diaza-bicyclo[3.2.1]octane-and 3,9-diaza- bicyclo[3.3.1]nonane-3-carboxylic acid ester derivatives useful as monoamine neurotransmitter re-uptake inhibitors. In other aspects the invention relates to the use of these co

NOVEL SUBSTITUTED DIAZABICYCLO DERIVATIVES AND THEIR USE AS MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITORS

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, (2008/06/13)

This invention relates to novel substituted diazabicyclo derivatives useful as monoamine neurotransmitter re-uptake inhibitors. In other aspects the invention relates to the use of these compounds in a method for therapy and to pharmaceutical compositions

NOVEL DIAZABICYCLIC ARYL DERIVATIVES AND THEIR MEDICAL USE

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Page/Page column 20, (2008/06/13)

This invention relates to novel diazabicyclic aryl derivatives which are found to be cholinergic ligands at the nicotinic acetylcholine receptors and modulators of the monoamine receptors and transporters. Due to their pharmacological profile the compound

NOVEL DIAZABICYCLIC ARYL DERIVATIVES AND THEIR MEDICAL USE

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Page/Page column 16, (2008/06/13)

This invention relates to novel diazabicyclic aryl derivatives, which are found to be cholinergic ligands at the nicotinic acetylcholine receptors and modulators of the monoamine receptors and transporters. Due to their pharmacological profile the compoun

Diazabicyclooctanes and diazabicycloheptanes

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, (2008/06/13)

Twelve analogs of diethylcarbamazine as prepared by acylation of 3- and 8-methyl-3,8-diazabicyclo[3.2.1]octane, 2-methyl-2,5-diazabicyclo[2.2.2]octane, and 2-methyl-2,5-diazabicyclo [2.2.1]heptane with diethylcarbamyl chloride, ethyl chloroformate, ethyl isocyanate, and cyclohexanecarbonyl chloride. These compounds are formally derived from diethylcarbamazine in possessing two- or one-carbon bridges over the piperazine ring. The compounds have utility as antifilarial agents and as bronchodilators.

Antifilarial agents. Diazabicyclooctanes and diazabicycloheptanes as bridged analogs of diethylcarbamazine

Sturm,Henry,Thompson,et al.

, p. 481 - 487 (2007/10/04)

Twelve analogs of diethylcarbamazine (DEC) were prepared by acylation of 3 and 8 methyl 3,8 diazabicyclo[3.2.1]octane, 2 methyl 2,5 diazabicyclo[2.2.2]octane, and 2 methyl 2,5 diazabicyclo[2.2.1]heptane with diethylcarbamyl chloride, ethyl chloroformate, ethyl isocyanate, and cyclohexanecarbonyl chloride. These compounds are formally derived from DEC in possessing two or one carbon bridges over the piperazine ring. When evaluated against Litomosoides carinii in the gerbil, all compounds strongly suppressed blood microfilaremia levels but did not affect the adult worms. Several compounds were nearly equivalent to DEC in activity. The results are discussed in terms of molecular model studies and receptor site theory.

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