85663-20-3 Usage
Uses
Used in Pharmaceutical Industry:
(3-(3,4-dichlorophenyl)indan-1-yl)-4-methylpiperazine is used as a pharmaceutical agent for its potential biological activity. (3-(3,4-dichlorophenyl)indan-1-yl)-4-methylpiperazine's structure, which includes a dichlorophenyl group, indicates that it may have applications in the development of new drugs, particularly those targeting specific receptors or pathways in the body.
Used in Agrochemical Industry:
In the agrochemical sector, (3-(3,4-dichlorophenyl)indan-1-yl)-4-methylpiperazine is used as a potential agrochemical agent. Its complex structure and the presence of the dichlorophenyl group may provide it with properties that could be harnessed for pest control, crop protection, or other agricultural applications.
Used in Chemical Research:
(3-(3,4-dichlorophenyl)indan-1-yl)-4-methylpiperazine is also used as a research compound in the field of chemistry. Its unique structure and potential biological activity make it an interesting subject for studying the relationships between chemical structure and biological function, which can lead to the discovery of new drugs or other applications.
Check Digit Verification of cas no
The CAS Registry Mumber 85663-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,6 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85663-20:
(7*8)+(6*5)+(5*6)+(4*6)+(3*3)+(2*2)+(1*0)=153
153 % 10 = 3
So 85663-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H22Cl2N2/c1-23-8-10-24(11-9-23)20-13-17(15-4-2-3-5-16(15)20)14-6-7-18(21)19(22)12-14/h2-7,12,17,20H,8-11,13H2,1H3
85663-20-3Relevant academic research and scientific papers
3-Phenyl-1-indanamines. Potential antidepressant activity and potent inhibition of dopamine, norepinephrine, and serotonin uptake
Bogeso,Christensen,Hyttel,Liljefors
, p. 1817 - 1828 (2007/10/02)
A series of 3-phenyl-1-indanamines was synthesized and tested for potential antidepressant activity and for inhibition of dopamine (DA), norepinephrine (NE), and serotonin (5-HT) uptake. Transisomers were generally potent inhibitors of DA, NE, and 5-HT up
Neuroleptic activity and dopamine-uptake inhibition in 1-piperazino-3-phenylindans
Bogeso
, p. 935 - 947 (2007/10/02)
A series of 1-piperazino-3-phenylindans was synthesized and tested for neuroleptic and thymoleptic activity. Neuroleptic activity was found only in trans racemates and was associated with one of the enantiomers only. The potent and long-acting neuroleptic compound trans-4-[3-(4-fluorophenyl)-6-(trifluoromethyl)indan-1-yl]-1-piperazineeth anol (Lu 18-012, tefludazine) was developed by systematic variation of structural components. Thymoleptic activity was optimized, especially with respect to dopamine-uptake inhibition. No geometrical stereoselectivity was found with regard to dopamine-uptake inhibition, but a high enantioselectivity could be demonstrated for both cis and trans racemates. The most potent compounds were 1-piperazino-3-(3,4-dichlorophenyl)indans with IC50 values of about 2 nM for inhibition of dopamine uptake.
