21391-99-1 Usage
Uses
Used in Pharmaceutical Industry:
α-Calacorene is used as an antimicrobial agent for its ability to inhibit the growth of certain microorganisms, which can be beneficial in the development of new antibiotics or antiseptic products.
Used in Cosmetic Industry:
α-Calacorene is used as an anti-inflammatory agent for its potential to reduce inflammation in skin care products, which can be particularly useful for soothing and treating skin conditions.
Used in Insect Repellent Development:
α-Calacorene is used as an insect repellent due to its potential to deter insects, which can be harnessed in the creation of natural and effective insect repellent products.
Used in Plant Defense Mechanisms Research:
α-Calacorene is used in studying plant defense mechanisms, as it plays a role in how plants protect themselves from pests and diseases, contributing to the broader understanding of botanical defense strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 21391-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,9 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21391-99:
(7*2)+(6*1)+(5*3)+(4*9)+(3*1)+(2*9)+(1*9)=101
101 % 10 = 1
So 21391-99-1 is a valid CAS Registry Number.
21391-99-1Relevant academic research and scientific papers
Adio, Adewale M.,von Reuss, Stephan H.,Paul, Claudia,Muhle, Hermann,Koenig, Wilfried A.
, p. 1245 - 1253 (2007)
Nine new amorphane sesquiterpenoids, (+)-7β-hydroxyamorpha-4,11-diene, (-)-9α-hydroxyamorpha-4,7(11)-diene, (-)-3α-hydroxyamorpha-4,7(11)-diene, (-)-3α-acetoxyamorpha-4,7(11)-diene, (-)-amorpha-4,7(11)-dien-3-one, (+)-2,8-epoxyamorpha-4,7(11)-diene, (+)-5,9-epoxyamorpha-3,7(11)-diene, (-)-2α-hydroxyamorpha-4,7(11)-diene and (-)-2β-acetoxyamorpha-4,7(11)-diene, were isolated from the essential oil of the liverwort Marsupella aquatica, collected near Gaschurn/Montafon, Austria. The isolated compounds and their chemical transformations were investigated using enantioselective GC and extensive spectroscopic studies (HRMS, 1H, 13C and 2D NMR). The absolute configuration of most of the isolated compounds were established by conversions to known compounds. In addition, 1H, and 13C NMR data of (-)-myltayl-4-ene are reported for the first time.
