28356-43-6 Usage
General Description
3-carbamoyl-1-hexylpyridinium is a chemical compound with the molecular formula C12H23N2O. It is a member of the pyridinium family and is often used as an intermediate in the production of other organic compounds. Its structure consists of a pyridine ring with a carbamoyl group and a hexyl chain attached to it. The compound has been studied for its potential use as an antimicrobial agent due to its ability to disrupt bacterial cell membranes. Additionally, it has also been investigated for its potential application in the development of novel drugs and pharmaceuticals. Overall, 3-carbamoyl-1-hexylpyridinium is a versatile chemical with various potential industrial and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 28356-43-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,5 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28356-43:
(7*2)+(6*8)+(5*3)+(4*5)+(3*6)+(2*4)+(1*3)=126
126 % 10 = 6
So 28356-43-6 is a valid CAS Registry Number.
28356-43-6Relevant articles and documents
Semisynthetic Enzymes: Characterization of Isomeric Flavopapains with Widely Different Catalytic Efficiencies
Slama, James T.,Radziejewski, Czestaw,Oruganti, SubbaRao,Kaiser, E. T.
, p. 6778 - 6785 (2007/10/02)
Flavopapain 6 has been prepared by alkylation of the active site cysteine-25 of papain with 8α-(bromoacetyl)-10-methylisoalloxazine.This semisynthetic enzyme was shown to serve as a catalyst for the oxidation of dihydronicotinamides, exhibiting saturation kinetics and up to 600-fold rate accelerations relative to a model flavin.This is contrasted to the behavior of flavopapain 9, the product of the modification of papain with 6α-(bromoacetyl)-10-methylisoalloxazine.In this case no catalytic rate enhancement compared to the behavior of a model compound is observed.Since the two isoalloxazines are isomeric, the differences in the activities of the semisynthetic enzymes are interpreted in terms of differences in the geometry of the flavin at the active site.It is also noted that flavopapain 6 can exhibit some chiral discrimination toward optically active dihydronicotinamides.
