61-67-6 Usage
Uses
Used in Pharmaceutical Industry:
4-deoxypyridoxine is used as a precursor for the synthesis of active pharmaceutical ingredients (APIs) due to its unique chemical structure and reactivity. It plays a crucial role in the development of new drugs targeting various diseases and conditions.
Used in Nutritional Supplements:
4-deoxypyridoxine is used as a key ingredient in nutritional supplements, particularly those aimed at promoting overall health and well-being. Its presence in these supplements helps maintain proper metabolic functions and supports the body's natural processes.
Used in Research and Development:
In the field of research and development, 4-deoxypyridoxine is used as a valuable compound for studying the structure and function of various biological molecules. Its unique properties make it an ideal candidate for investigating the interactions between different biomolecules and their potential applications in medicine and biotechnology.
Used in Cosmetics Industry:
4-deoxypyridoxine is also used in the cosmetics industry as an active ingredient in various skincare and hair care products. Its presence in these products helps improve the overall health and appearance of the skin and hair, making it a sought-after component in the formulation of cosmetics.
Synthesis Reference(s)
The Journal of Organic Chemistry, 26, p. 596, 1961 DOI: 10.1021/jo01061a608
Check Digit Verification of cas no
The CAS Registry Mumber 61-67-6 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61-67:
(4*6)+(3*1)+(2*6)+(1*7)=46
46 % 10 = 6
So 61-67-6 is a valid CAS Registry Number.
61-67-6Relevant academic research and scientific papers
Studies on anticoccidial agents. 1. Synthesis and anticoccidial activity of 4 deoxypyridoxol and its esters
Morisawa,Kataoka,Watanabe,Kitano,Matsuzawa
, p. 1083 - 1086 (2007/10/04)
Methods for syntheses of 4 deoxypyridoxine and 2 ethyl 2 demethylpyridoxine from pyridoxine were developed. α5 O Monoacyl 4 deoxypyridosines were, in general, obtained by selective hydrolysis of 3,α5 O diacyl 4 deoxypyridoxines. 4 Deoxypyridoxine and its esters showed anticoccidial activity against Eimeria acervulina. (19 references.)