625109-32-2 Usage
Chemical structure
A complex molecular structure containing a chloroacetyl group, a furan ring, a methylphenyl group, and a dihydropyrazole ring.
Chloroacetyl group
A functional group with a chlorine atom attached to an acetyl group, which can participate in various chemical reactions.
Furan ring
A heterocyclic organic compound consisting of a four-membered ring with one oxygen atom, which can be involved in various chemical reactions.
Methylphenyl group
A phenyl group (a six-membered aromatic ring) with a methyl group attached, which can influence the compound's reactivity and properties.
Dihydropyrazole ring
A five-membered heterocyclic ring with two nitrogen atoms and two carbon atoms, which can be involved in various chemical reactions.
Potential applications
The compound may be used in pharmaceutical research for drug development due to its unique structure and properties.
Organic synthesis
The compound could be used as a building block for more complex compounds in organic synthesis.
Diverse applications
Due to its complex structure, the compound may have diverse applications in various chemical and biological processes.
Chemical reactivity
The presence of multiple functional groups and structural elements gives the compound a diverse range of potential chemical reactivity.
Research potential
The compound's unique structure and properties make it an interesting candidate for further research in both chemical and biological fields.
Check Digit Verification of cas no
The CAS Registry Mumber 625109-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,5,1,0 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 625109-32:
(8*6)+(7*2)+(6*5)+(5*1)+(4*0)+(3*9)+(2*3)+(1*2)=132
132 % 10 = 2
So 625109-32-2 is a valid CAS Registry Number.
625109-32-2Relevant articles and documents
3-Aryl-5-furylpyrazolines and their biological activities
Cetin, Ahmet,Cansiz,Digrak
, p. 345 - 347 (2003)
Aryl-furyl substituted pyrazolines 2a-c and 4a-c were prepared by the reaction of α,βunsaturated carbonyl compounds with hydrazine or phenyl hydrazine. N-chloroacetyl derivatives 3a-c were obtained by the N-acetylation of 2a-c. The antibacterial activities of synthesized pyrazolines were examined by employing the disk-diffusion technique. All synthesized compounds showed antibacterial effects in 1200 μg concentration.
