Welcome to LookChem.com Sign In|Join Free
  • or
The chemical compound "5-(α-hydroxy-α-2-pyridylbenzyl)-N-methyl-7-(α-2-pyridylbenzylidene)-5-norbornene-2,3-dicarboximide" is a complex organic molecule with a unique structure. It features a norbornene core, which is a type of bicyclic compound with a seven-membered ring fused to a two-membered ring. The molecule is adorned with two pyridylbenzyl groups, one of which is hydroxylated and the other forms a benzylidene with the norbornene core. Additionally, it contains a methyl group attached to the nitrogen atom and a dicarboximide functional group, which is a derivative of a dicarboxylic acid where the hydroxyl groups are replaced by imido groups. 5-(α-hydroxy-α-2-pyridylbenzyl)-N-methyl-7-(α-2-pyridylbenzylidene)-5-norbornene-2,3-dicarboximide is characterized by its intricate arrangement of functional groups and may have potential applications in various fields due to its specific chemical properties.

6434-24-8

Post Buying Request

6434-24-8 Suppliers

Recommended suppliers

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

6434-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6434-24-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6434-24:
(6*6)+(5*4)+(4*3)+(3*4)+(2*2)+(1*4)=88
88 % 10 = 8
So 6434-24-8 is a valid CAS Registry Number.

6434-24-8Downstream Products

6434-24-8Relevant academic research and scientific papers

Design and synthesis of prodrugs of the rat selective toxicant norbormide

Rennison, David,Laita, Olivia,Bova, Sergio,Cavalli, Maurizio,Hopkins, Brian,Linthicum, Darwin S.,Brimble, Margaret A.

, p. 3997 - 4011 (2012)

Norbormide [5-(α-hydroxy-α-2-pyridylbenzyl)-7-(α-2- pyridylbenzylidene)-5-norbornene-2,3-dicarboximide] (NRB), an existing but infrequently used rodenticide, is known to be uniquely toxic to rats but relatively harmless to other rodents and mammals. However, one major drawback of NRB as a viable rodenticide relates to an evolutionary aversion developed by the rat leading to sub-lethal dosing due to either its unpleasant 'taste' or rapid onset of effects. A series of NRB prodrugs were prepared in an effort to 'mask' this acute response. Their synthesis and biological evaluation (in vitro vasoconstrictory activity, in vitro hydrolytic and enzymatic stability and lethality/palatability in vivo) is described. Compound 19 displayed the most promising profile with respect to a delay in the onset of symptoms and was subsequently demonstrated to be significantly more palatable to rats.

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 6434-24-8