Welcome to LookChem.com Sign In|Join Free

CAS

  • or

51862-97-6

Post Buying Request

51862-97-6 Suppliers

Recommended suppliersmore

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

51862-97-6 Usage

General Description

N-Acetyl-N-(2-oxopropyl)acetamide, also known as N-Acetylglutamate, is a chemical compound that is derived from acetic acid and has important biological functions in the human body. It plays a key role in the urea cycle, which is responsible for the detoxification of ammonia in the liver. N-Acetyl-N-(2-oxopropyl)acetamide is a precursor for the synthesis of urea, an important waste product that is excreted from the body through urine. Additionally, this chemical compound has potential therapeutic applications, particularly in the treatment of urea cycle disorders and hyperammonemia, which are conditions characterized by the accumulation of ammonia in the bloodstream. Overall, N-Acetyl-N-(2-oxopropyl)acetamide is a crucial component in the maintenance of nitrogen metabolism and plays a significant role in human health.

Check Digit Verification of cas no

The CAS Registry Mumber 51862-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,6 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51862-97:
(7*5)+(6*1)+(5*8)+(4*6)+(3*2)+(2*9)+(1*7)=136
136 % 10 = 6
So 51862-97-6 is a valid CAS Registry Number.

51862-97-6Relevant articles and documents

Synthesis and conformational analysis of an expanded cyclic ketoxime-hexapeptide

Lamping, Matthias,Grell, Yvonne,Geyer, Armin

, p. 228 - 235 (2016/04/19)

In this work the synthesis of a linear hexapeptide with a hydroxylamine functionality at the N-terminus and a ketone instead of the carboxylic acid at the C-terminus is described. Cyclization by ketoxime formation yields the 19-membered ring-expanded cyclic hexapeptide cyclo[Goly-Val-Ala-Pro-Leu-Kly] which adopts a main conformer with two intramolecular hydrogen bonds. The hydrolytic stability of a ketoxime lies between the inert amide and the labile imine. The substitution of an amide bond for an iminium bond transforms the irreversible macrocyclization into a reversible process, but macrocyclic imines are difficult to isolate because they are prone to hydrolysis. The enhanced chemical stability of the ketoxime justifies its application in ligation protocols. The detailed NMR analysis of a ketoxime linkage presented here identifies its local conformational preferences in a constrained peptide environment.

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

What can I do for you?
Get Best Price

Get Best Price for 51862-97-6