4184-34-3 Usage
Uses
Used in Pharmaceutical Industry:
(24E)-3β-Hydroxy-9β,19-cyclo-5α-lanost-24-en-26-oic acid is used as a pharmaceutical compound for its potential biological activity. (24E)-3β-Hydroxy-9β,19-cyclo-5α-lanost-24-en-26-oic acid's structure, including its hydroxy and oic acid groups, may contribute to its interaction with biological systems, making it a candidate for drug development and therapeutic applications.
Used in Chemical Research:
In the field of chemical research, (24E)-3β-Hydroxy-9β,19-cyclo-5α-lanost-24-en-26-oic acid serves as a subject of study for understanding the properties and reactions of lanostane steroids. Its unique cyclo structure and functional groups provide insights into the chemistry of natural products and their potential applications in various industries.
Used in Cosmetic Industry:
(24E)-3β-Hydroxy-9β,19-cyclo-5α-lanost-24-en-26-oic acid may be utilized in the cosmetic industry due to its potential effects on skin health and its ability to interact with biological systems. (24E)-3β-Hydroxy-9β,19-cyclo-5α-lanost-24-en-26-oic acid's polarity and solubility properties could be harnessed to create formulations with beneficial properties for skincare products.
Check Digit Verification of cas no
The CAS Registry Mumber 4184-34-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,8 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4184-34:
(6*4)+(5*1)+(4*8)+(3*4)+(2*3)+(1*4)=83
83 % 10 = 3
So 4184-34-3 is a valid CAS Registry Number.
4184-34-3Relevant academic research and scientific papers
Reactions of Triterpenes: Part III - Partial Synthesis of 3β-Hydroxycycloart-24-en-26-al from Cycloart-24-ene-3β,26-diol
Anjaneyulu, V.,Prasad, K. Harischandra
, p. 1075 - 1076 (2007/10/02)
Oxidation of cycloart-24-ene-3β,26-diol (I) with DDQ or Ag2CO3/SiO2 in dry benzene gives only 3β-hydroxycycloart-24-en-26-al (II) whereas CrO3/pyridine oxidation of I yields II, mangiferonic acid (IV) and mangiferolic acid (V), besides a new ketoaldehyde (III).
