465-02-1 Usage
Uses
Used in Pharmaceutical Industry:
GERMANICOL is used as a pharmaceutical agent for its anti-inflammatory, antitumor, antiviral, and antimicrobial properties. Its bioactive properties make it a promising candidate for the development of new drugs and therapies.
Used in Cosmetic Industry:
In the cosmetic industry, GERMANICOL is used as an active ingredient for its skin regenerative, anti-aging, and wound healing properties. It is incorporated into various skincare products to promote healthy and youthful skin.
Used in Food Industry:
GERMANICOL is used as a food additive for its emulsifying, stabilizing, and antioxidant properties. It helps improve the texture, taste, and shelf life of various food products.
Used in Nanotechnology:
In the field of nanotechnology, GERMANICOL is used for the synthesis of nanoparticles with potential applications in drug delivery, imaging, and diagnostics. Its unique properties allow for the development of targeted and efficient nanosystems.
Used in Agriculture:
GERMANICOL is used in agriculture as a natural pesticide and growth promoter. Its antimicrobial and antifungal properties help protect crops from diseases and pests, while also promoting healthy growth.
Check Digit Verification of cas no
The CAS Registry Mumber 465-02-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 465-02:
(5*4)+(4*6)+(3*5)+(2*0)+(1*2)=61
61 % 10 = 1
So 465-02-1 is a valid CAS Registry Number.
InChI:InChI=1/C30H50O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h19-20,22-24,31H,9-18H2,1-8H3/t20-,22+,23-,24+,27-,28+,29-,30-/m1/s1
465-02-1Relevant academic research and scientific papers
A short enantioselective total synthesis of the fundamental pentacyclic triterpene lupeol
Surendra, Karavadhi,Corey
supporting information; experimental part, p. 13928 - 13929 (2009/12/25)
(Chemical Equation Presented) The first enantioselective synthesis of lupeol has been developed by applying two carefully crafted cation-π cyclization stages to generate the pentacyclic structure with complete stereocontrol. The synthesis (Scheme 1) is no
Arabidopsis thaliana LUP1 converts oxidosqualene to multiple triterpene alcohols and a triterpene diol
Segura, Michael J. R.,Meyer, Michelle M.,Matsuda, Seiichi P. T.
, p. 2257 - 2259 (2007/10/03)
lupeol lupeol, germanicol, synthase β-amyrin, taxasterol, oxidosqualene → ψ-taraxasterol, and 3,20-dihydroxylupane The Arabidopsis thaliana LUP1 gene encodes an enzyme that converts oxidosqualene to pentacyclic triterpenes. Lupeol and β-amyrin were previously reported as LUP1 products. Further investigation described here uncovered the additional products germanicol, taraxasterol, ψ-taraxasterol, and 3,20-dihydroxylupane. These results suggest that the 80 known C30H50O compounds that are structurally consistent with being oxidosqualene cyclase products may be derived from fewer than 80 enzymes and that some C30H52O2 compounds may be direct cyclization products of oxidosqualene.
