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PIMOZIDE CAS NO.2062-78-4

Min.Order Quantity:
1 Kilogram
Purity:
98%
Port:
China Main Port
Payment Terms:
L/C,D/A,D/P,T/T,MoneyGram,Other

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Product Details

Keywords

  • PIMOZIDE
  • 2062-78-4
  • C28H29F2N3O

Quick Details

  • ProName: PIMOZIDE
  • CasNo: 2062-78-4
  • Molecular Formula: C28H29F2N3O
  • Appearance: powder
  • Application: 2062-78-4
  • DeliveryTime: Within 3-7days
  • PackAge: As requested
  • Port: China Main Port
  • ProductionCapacity: 300 Kilogram/Day
  • Purity: 98%
  • Storage: 2-8°C
  • Transportation: By air or by sea
  • LimitNum: 1 Kilogram

Superiority

pimozide basic information
product name: pimozide
synonyms: pimozide;1-(1-(4,4-bis(p-fluorophenyl)butyl)-4-piperidyl)-2-benzimidazolinon;1-(1-(4,4-bis(p-fluorophenyl)butyl)-4-piperidyl)-2-benzimidazolinone;1-(4,4-bis(p-fluorophenyl)butyl)-4-(2-oxo-1-benzimidazolinyl)piperidine;mcn-jr-6238;orap;1-[1-(4,4-bis[4-fluorophenyl]butyl)-4-piperidinyl]-1,3-dihydro-2h-benz-imidazol-2-one;3-(1-(4,4-bis(4-fluorophenyl)butyl)-4-piperidyl)-1h-benzimidazol-2-one
cas: 2062-78-4
mf: c28h29f2n3o
mw: 461.55
einecs: 218-171-7
product categories: organics;dopamine receptor;orap;inhibitors
mol file: 2062-78-4.mol
pimozide structure
pimozide chemical properties
storage temp. 2-8°c
solubility dmso: 18 mg/ml
cas database reference 2062-78-4(cas database reference)
safety information
hazard codes xn
risk statements 22
safety statements 36
ridadr 3249
wgk germany 3
rtecs de1750000
hazardclass 6.1(b)
packinggroup iii
pimozide usage and synthesis
usage antipsychotic
usage used for the suppression of motor and phonic tics in patients with tourette's disorder who have failed to respond satisfactorily to standard treatment.
definition chebi: a member of the class of benzimidazoles that is 1,3-dihydro-2h-benzimidazol-2-one in which one of the nitrogens is substituted by a piperidin-4-yl group, which in turn is substituted on the nitrogen by a 4,4-bis(p-fluorophen l)butyl group.
biological activity dopamine d 2 -receptor antagonist and antipsychotic which binds with very high affinity to the cloned rat 5-ht 7 receptor (k i = 0.5 nm).

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