Welcome to LookChem.com Sign In|Join Free
  • or
"Z,1-Acetyl-4-(5-fluoro-2-hydroxybenzoyl)piperidine O-acetyloxime" is a complex organic chemical compound with the molecular formula C18H20FNO5. It is characterized by a piperidine ring, which is a six-membered cyclic amine, and a 5-fluoro-2-hydroxybenzoyl group, indicating the presence of a fluorine atom and a hydroxyl group on the benzene ring. The compound also features an acetoxymethylene group, which is a double bond between carbon and oxygen with an acetate group attached. This chemical is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of certain drugs. Its structure and properties make it a compound of interest for researchers in medicinal chemistry, due to its ability to form stable derivatives and its potential to influence biological activity.

84163-76-8

Post Buying Request

84163-76-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

84163-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84163-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,6 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84163-76:
(7*8)+(6*4)+(5*1)+(4*6)+(3*3)+(2*7)+(1*6)=138
138 % 10 = 8
So 84163-76-8 is a valid CAS Registry Number.

84163-76-8Relevant academic research and scientific papers

Synthesis and Neuroleptic Activity of 3-(1-Substituted-4-piperidinyl)-1,2-benzisoxazoles

Strupczewski, Joseph T.,Allen, Richard C.,Gardner, Beth Ann,Schmid, Blaine L.,Stache, Ulrich,et al.

, p. 761 - 769 (2007/10/02)

The synthesis of a series of 3-(1-substituted-4-piperidinyl)-1,2-benzisoxazoles is described.The neuroleptic activity of the series was evaluated by utilizing the climbing mice assay and inhibition of spiroperidol binding.Structure-activity relationships were studied by variation of the substituent on the benzisoxazole ring with concomitant variation of four different 1-piperidinyl substituents.Maximum neuroleptic activity was realized when there was a 6-fluoro substituent on the benzisoxazole ring.The 1-piperidinyl substituent appeared less significant, although in most cases, the (1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl group imparted maximum potency.The most potent compound in both assays was 6-fluoro-3--4-piperidinyl>-1,2-benzisoxazole (11b).

3-(4-Piperidyl)-1,2-benzisoxales

-

, (2008/06/13)

Novel 3-(4-piperidyl)-1,2-benzisoxazoles, intermediates and processes for the preparation thereof, and methods for alleviating pain utilizing compounds or compositions thereof are disclosed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 84163-76-8