73256-82-3 Usage
General Description
Isobicyclogermacrenal is a naturally occurring sesquiterpene compound found in various plant species. It is known for its strong odor, reminiscent of ginger and citrus. Isobicyclogermacrenal is commonly used in the perfume industry for its unique scent. It also exhibits potential anti-inflammatory and antioxidant properties, making it a subject of interest in the field of natural medicine. Studies have shown that isobicyclogermacrenal has the potential to inhibit the production of inflammatory mediators and scavenge free radicals, suggesting a possible role in the treatment of inflammatory and oxidative stress-related conditions. Overall, isobicyclogermacrenal is a versatile compound with both practical and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 73256-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,5 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73256-82:
(7*7)+(6*3)+(5*2)+(4*5)+(3*6)+(2*8)+(1*2)=133
133 % 10 = 3
So 73256-82-3 is a valid CAS Registry Number.
73256-82-3Relevant articles and documents
Structures and Conformations of (-)-Isobicyclogermacrenal and (-)-Lepidozenal, Two Key Sesquiterpenoids of the cis- and trans-10,3-Bicyclic Ring Systems, from the Liverwort Lepidozia vitrea: X-Ray Crystal Structure Analysis of the Hydroxy Derivative of (-)-Isobicyclogermacrenal
Matsuo, Akihiko,Nozaki, Hiroshi,Kubota, Naoji,Uto, Seiryo,Nakayama, Mitsuru
, p. 203 - 214 (2007/10/02)
The structures and absolute configurations of the two sesquiterpene aldehydes, (-)-isobicyclogermacrenal (1) and (-)-lepidozenal (2), which were isolated from the liverwort Lepidozia vitrea, have been determined on the basis of chemical and spectroscopic evidence to be (6R,7S)-6,11-cyclogermacra-1(10)E,4E-dien-14-al and (6R,7R)-lepidoza-1(10)E,4E-dien-14-al, cosisting of the cis- and trans-10,3-bicyclic ring systems.The structure of the former (1) has been confirmed by a single-crystal X-ray analysis of its hydroxy derivative (7).The molecular conformations, biogenetical features, and biological activity are also described.
