852109-69-4 Usage
Structure
Complex organic compound with a spirocyclic structure
Ring System
Contains a 1,6-dioxaspiro ring system
Moiety
Contains a 2-[(4-chlorophenyl)methylene]-9-ethyl moiety
Conformation
Exists in the Z conformation, indicating a specific arrangement of functional groups around the double bond
Potential Applications
May have potential applications in medicinal chemistry as a scaffold for the development of new pharmaceutical compounds
Unique Structure
Its unique structure and functional groups could make it interesting for further studies in organic synthesis and chemical reactivity
Functional Groups
Contains a carbonyl group, a double bond, a chlorine atom, and an ethyl group
Stereochemistry
The Z conformation indicates the stereochemistry of the double bond, with the chlorine atom and the ethyl group on the same side of the molecule
Reactivity
The presence of the carbonyl group and the double bond suggests that the compound may be reactive towards nucleophiles and electrophiles, respectively.
Check Digit Verification of cas no
The CAS Registry Mumber 852109-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,1,0 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 852109-69:
(8*8)+(7*5)+(6*2)+(5*1)+(4*0)+(3*9)+(2*6)+(1*9)=164
164 % 10 = 4
So 852109-69-4 is a valid CAS Registry Number.
852109-69-4Relevant academic research and scientific papers
Molecular diversity of tonghaosu: Synthesis of lactam-containing tonghaosu analogs
Yin, Biao-Lin,Yang, Zheng-Min,Hu, Tai-Shan,Wu, Yu-Lin
, p. 1995 - 2000 (2007/10/03)
A new type of tonghaosu analogs containing spiroketal and lactam functionality was synthesized from methyl 2-furoate and amino alcohols. The stereoselective control of spiroketal chirality was also explored.
