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Azabuperone, also known as 1-(4-fluorophenyl)-4-[4-(2-piperidin-1-yl-2-oxoethyl)piperidin-1-yl]butan-1-one, is a synthetic chemical compound belonging to the class of butyrophenone neuroleptics. It is primarily used as an antipsychotic medication, exhibiting its effects by blocking dopamine receptors in the brain, particularly D2 receptors, which are associated with the positive symptoms of schizophrenia and other psychotic disorders. Azabuperone has been studied for its potential therapeutic applications in treating various mental health conditions, but it is not as widely used as other butyrophenone drugs due to its side effects and the availability of alternative treatments.

2856-81-7

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2856-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2856-81-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2856-81:
(6*2)+(5*8)+(4*5)+(3*6)+(2*8)+(1*1)=107
107 % 10 = 7
So 2856-81-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H23FN2O/c18-15-7-5-14(6-8-15)17(21)4-2-9-19-11-12-20-10-1-3-16(20)13-19/h5-8,16H,1-4,9-13H2

2856-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3,4,6,7,8,8a-hexahydro-1H-pyrrolo[1,2-a]pyrazin-2-yl)-1-(4-fluorophenyl)butan-1-one

1.2 Other means of identification

Product number -
Other names Azabuperona [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:2856-81-7 SDS

2856-81-7Downstream Products

2856-81-7Relevant academic research and scientific papers

Studies in Potential Filaricides: Part XIII - Synthesis of 1,4-Diazabicyclononanes, 1,4-Diazabicyclodecanes and 1,4-Diazabicycloundecanes as diethylcarbamazine Analogs

Shukla, U. K.,Khanna, J. M.,Sharma, Satyavan,Anand, Nitya,Chatterjee, R. K.,Sen, A. B.

, p. 664 - 668 (2007/10/02)

1,4-Diazabicyclononanes (13 - 20), 1,4-diazabicyclodecanes (21 - 28), 1,4-diazabicycloundecanes (29 - 34), 1,4-diazabicyclononan-5-ones (37 - 41) and 1,4-diazabicyclodecan-5-ones (42 - 44) having alkyl and acyl substituents at 4-position have been synthesized and evaluated for their filaricidal activity against Litomasoides carinii infection in cotton rats.Except 4-diethylcarbamoyl-1,4-diazabicyclononane (13), which exhibits significant activity, being about 3/5th as active as the standard diethylcarbamazine (DEC), none of the other compounds shows any activity against adult worms.The results have been rationalised in terms of critical bulk around the N-1 of the piperazine ring of DEC.From this work and earlier published results it appears that both axial and equatorial N-CH3 bonds in DEC are acceptable for activity.

Process for the preparation of tertiary amines

-

, (2008/06/13)

Certain tertiary amines useful as pharmaceuticals are prepared in improved yields by condensing a cyclic secondary amine with a primary alkyl halide in an aqueous medium in the presence of an acid acceptor.

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