138540-99-5 Usage
Uses
Used in Pharmaceutical Industry:
Garlicin is used as an antimicrobial agent for its ability to combat various types of bacteria, fungi, and viruses, making it a valuable component in the development of natural antibiotics and antifungal medications.
Used in Cardiovascular Health Applications:
Garlicin is used as a cholesterol-lowering and blood pressure-reducing agent for its capacity to improve cardiovascular health, reducing the risk of heart diseases and strokes.
Used in Immune System Support:
Garlicin is used as an immune-boosting agent for its ability to enhance the body's natural defenses against infections and diseases.
Used in Anti-Inflammatory Applications:
Garlicin is used as an anti-inflammatory agent for its potential to reduce inflammation in the body, which can help alleviate symptoms of various inflammatory conditions.
Used in Anticancer Research:
Garlicin is used as a subject of research for its potential anticancer effects, with studies exploring its ability to inhibit the growth and spread of cancer cells.
Used in Dietary Supplements:
Garlicin is used as an ingredient in dietary supplements for its wide range of health benefits, including its antimicrobial, cardiovascular, immune-boosting, and anti-inflammatory properties.
Check Digit Verification of cas no
The CAS Registry Mumber 138540-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,4 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138540-99:
(8*1)+(7*3)+(6*8)+(5*5)+(4*4)+(3*0)+(2*9)+(1*9)=145
145 % 10 = 5
So 138540-99-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O4/c9-5-1-2-6(10)7-4(5)3-12-8(7)11/h4-7,9-10H,1-3H2
138540-99-5Relevant academic research and scientific papers
Synthesis of 4,7-Dihydroxyperhydroisobenzofuran-1-one and Comparison with Zwergal's Structure of "Garlicin"
Nour, Reema Abdel,Schneider, Karin,Urban, Ernst
, p. 383 - 386 (2007/10/02)
The Diels-Alder reaction of 2-(benzoyloxy)furan (2) with maleic anhydride leads to the adduct 3 which, on hydrogenation, affords the exo anhydride 4a (71percent) and endo anhydride 4b (2.4percent).The regioselective reduction of 4a and 4b with NaBH4 leads
Xn:Harmful;
