74671-13-9 Usage
Molecular structure
The compound contains two pyrrole ring structures, which are five-membered heterocyclic aromatic rings with one nitrogen atom. The nitrogen atom in the pyrrole ring contributes to the compound's aromaticity and stability.
Functional groups
The compound has various functional groups, including amide, amino, carbonyl, and imino groups. These groups are responsible for the compound's reactivity and its ability to form various chemical bonds.
Amide group
The presence of the amide group (-CONH2) provides the compound with hydrogen bonding capabilities, which can influence its solubility and reactivity with other molecules.
Amino group
The amino group (-NH2) is a basic functional group that can participate in acid-base reactions and form hydrogen bonds, affecting the compound's solubility and reactivity.
Carbonyl group
The carbonyl group (C=O) is a polar functional group that can engage in hydrogen bonding and serve as a site for nucleophilic attack in chemical reactions.
Imino group
The imino group (-NH) is similar to the amino group but has a double bond between the nitrogen and hydrogen atoms, which can participate in various chemical reactions.
Substituents
The compound has multiple substituents, including acetyl, methyl, and iminopropyl groups, which contribute to its complex structure and properties.
Acetyl group
The acetyl group (-COCH3) is an alkyl group derived from acetic acid, which can influence the compound's reactivity and solubility.
Methyl group
The methyl group (-CH3) is a small alkyl group that can affect the compound's steric properties and reactivity.
Iminopropyl group
The iminopropyl group (-CH2CH2NH-) is a functional group derived from an amino acid, which can participate in various chemical reactions and contribute to the compound's reactivity.
Salt form
The compound is typically found in its dihydrochloride salt form, which enhances its stability and solubility in aqueous solutions. This salt form is achieved by reacting the compound with hydrochloric acid (HCl), resulting in the formation of a water-soluble salt.
Check Digit Verification of cas no
The CAS Registry Mumber 74671-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,7 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74671-13:
(7*7)+(6*4)+(5*6)+(4*7)+(3*1)+(2*1)+(1*3)=139
139 % 10 = 9
So 74671-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C24H32N12O4.2ClH/c1-34-11-14(7-16(34)21(38)29-5-4-19(25)26)32-23(40)18-8-15(12-36(18)3)33-22(39)17-6-13(10-35(17)2)31-20(37)9-30-24(27)28;;/h6-8,10-12H,4-5,9H2,1-3H3,(H3,25,26)(H,29,38)(H,31,37)(H,32,40)(H,33,39)(H4,27,28,30);2*1H
74671-13-9Relevant academic research and scientific papers
Structure-Activity Relationships of Pyrrole Amidine Antiviral Antibiotics. 2. Preparation of Mono- and Tripyrrole Derivatives of Congocidine
Bialer, Meir,Yagen, Boris,Mechoulam, Raphael,Becker, Yechiel
, p. 1144 - 1148 (2007/10/02)
Representatives of three types of congocidine (1) analogues were synthesized.These were tested for cytotoxicity, inhibition of herpes simplex virus (HSV) replication in cultured cells, and effects on the synthesis of HSV DNA in isolation nuclei in vitro, as well as on DNA synthesis by purified HSV-DNA polymerase.All synthesized tripyrrole derivatives of congocidine were less cytotoxic and more active than the parent drug in all the three antiviral tests.
