677752-10-2 Usage
Class
Spiro compounds
The compound has two rings joined by a single atom, forming a unique spirocyclic structure.
Structure
Six-membered ring fused to a five-membered ring with an oxygen atom in the bridge
The spirocyclic structure consists of one six-membered ring and one five-membered ring connected by an oxygen atom.
Substituents
Methyl group and methylene group attached to the six-membered ring
The compound has additional functional groups that contribute to its unique properties.
Classification
Terpene
Terpenes are a class of natural products with diverse biological activities.
Stereochemical configuration
(4S,5S,6R)-notation
This notation indicates the arrangement of substituent groups around the spirocyclic core, which is essential for understanding the compound's properties and potential applications.
Potential applications
Fragrance and flavor industries
Due to its unique structure and potential biological activities, the compound may be useful in creating new fragrances and flavors.
Biological activities
Not specified in the material provided
While the compound is classified as a terpene, which generally have diverse biological activities, the specific activities for 1,3-Dioxaspiro[4.4]nonan-6-ol,2,2,4-trimethyl-7-methylene-,(4S,5S,6R)-(9CI) are not mentioned in the provided material.
Check Digit Verification of cas no
The CAS Registry Mumber 677752-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,7,5 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 677752-10:
(8*6)+(7*7)+(6*7)+(5*7)+(4*5)+(3*2)+(2*1)+(1*0)=202
202 % 10 = 2
So 677752-10-2 is a valid CAS Registry Number.
677752-10-2Relevant academic research and scientific papers
Synthesis and structure of diastereomers of pentenocin B produced by Trichoderma hamatum FO-6903
Ohira, Susumu,Fujiwara, Hiroyuki,Maeda, Kiyomi,Habara, Masaharu,Sakaedani, Naomi,Akiyama, Megumi,Kuboki, Atsuhito
, p. 1639 - 1641 (2007/10/03)
All diastereomers of pentenocin B, an inhibitor of interleukin-1β converting enzyme produced by Trichoderma hamatum FO-6903, were synthesized in chiral forms starting from L-threonine. Absolute configurations of natural pentenocin B were clarified to be 4S, 5R, and 6R.
