5809-54-1 Usage
Functional Groups
Amino groups: Provide basicity and potential for hydrogen bonding
Carbonitrile group: Offers reactivity for various synthetic transformations
Methylsulfanyl group: Imparts lipophilicity and modulates compound's physicochemical properties
Trimethoxyphenyl moiety: Adds complexity and potential for interactions with biological targets
Applications
Medicinal chemistry: Potential for drug design and development
Pharmaceutical research: Exploration of pharmacological activities and structure-activity relationships
Chemical Characteristics
Multiple heterocyclic rings: Contribute to compound's structural diversity and potential for varied interactions
Nitrogen atoms: Enhance compound's versatility and reactivity in organic synthesis
Potential Research Areas
Organic chemistry: Investigation into synthetic methodologies and chemical transformations
Pharmacology: Evaluation of biological activities and therapeutic potential
Check Digit Verification of cas no
The CAS Registry Mumber 5809-54-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,0 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5809-54:
(6*5)+(5*8)+(4*0)+(3*9)+(2*5)+(1*4)=111
111 % 10 = 1
So 5809-54-1 is a valid CAS Registry Number.
5809-54-1Relevant academic research and scientific papers
STERICALLY SCREENED HALOGENOCYCLOBUTANONES. V. CYCLOPROPYL-SUBSTITUTED OLEFINS IN REACTION WITH DICHLOROKETENE
Bessmertnykh, A. G.,Bubnov, Yu. N.,Voevodskaya, T. I.,Donskaya, N. A.,Zykov, A. Yu.
, p. 2027 - 2033 (2007/10/02)
Trisubstituted olefins containing various numbers of cyclopropyl substituents were synthesized.They react with dichloroketene regio- and stereospecifically, giving high yields of dichlorocyclobutanones.The introduction of electron-withdrawing chlorine atoms into one of the three-carbon rings leads to only a small decrease in the reactivity of the double bond in this reaction.
