Welcome to LookChem.com Sign In|Join Free
  • or
m-(Trifluoromethyl)phenylalanine hydrochloride is a chemical compound with the molecular formula C10H12ClF3NO2. It is a derivative of the naturally occurring amino acid phenylalanine, featuring a trifluoromethyl group (-CF3) at the meta (3rd) position of the phenyl ring. This modification imparts unique properties to the molecule, such as increased lipophilicity and potential for enhanced binding affinity in biological systems. The hydrochloride salt form of the compound is often used to improve its solubility and stability. m-(Trifluoromethyl)phenylalanine hydrochloride has potential applications in medicinal chemistry, particularly in the development of novel drugs targeting various diseases, as well as in the synthesis of other complex organic molecules.

3832-76-6

Post Buying Request

3832-76-6 Suppliers

Recommended suppliers

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

3832-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3832-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,3 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3832-76:
(6*3)+(5*8)+(4*3)+(3*2)+(2*7)+(1*6)=96
96 % 10 = 6
So 3832-76-6 is a valid CAS Registry Number.

3832-76-6Relevant academic research and scientific papers

Inactivation of Leukocyte Elastase by Aryl Azolides and Sulfonate Salts. Structure-Activity Relationship Studies

Groutas, W. C.,Brubaker, M. J.,Zandler, M. E.,Mazo-Gray, V.,Rude, S. A.,et al.

, p. 1302 - 1305 (2007/10/02)

The inhibitory activity of a series of aryl azolides and sulfonate salts toward human leukocyte elastase is reported.Several of the compounds were found to be potent inhibitors of the enzyme.Active compounds were obtained only when the specificity group and the reactive moiety were separated by a two-carbon chain.The introduction of hydrophobic groups enhanced the inhibitory activity of these compounds, with the exception of the sulfonate salts.The nature of the leaving group had had a profound effect on inhibitory activity, with compounds 23 and 26 being the most active (kobsd/ = 11722 and 13500 M-1 s-1, respectively).

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 3832-76-6