7441-35-2 Usage
Chemical family
Carboxylic acids It belongs to the family of carboxylic acids, which are organic compounds containing a carboxyl group (-COOH).
Organic compound
Yes It is an organic compound, as it contains carbon and hydrogen atoms.
Hydrocarbon chain length
11 carbon atoms The compound has a long hydrocarbon chain with 11 carbon atoms.
Terminal group
Carboxylic acid (-COOH) The hydrocarbon chain ends with a carboxylic acid group, which is characteristic of carboxylic acids.
Amino functionality
Ethylamino group An ethylamino group is attached to the carbon chain, adding amino functionality to the compound.
Amino acid derivative
Yes The presence of the ethylamino group makes it an amino acid derivative.
Applications
Pharmaceutical synthesis, surface-active agents, and polymers It is used as a precursor in the synthesis of various pharmaceuticals and is also involved in the production of surface-active agents and polymers.
Industrial and research applications
Yes Its properties and structure make it useful in various industrial and research applications.
Solubility
Generally soluble in organic solvents Like most organic compounds, it is likely to be soluble in organic solvents such as ethanol, methanol, or acetone.
Melting point
Varies depending on the specific compound The melting point of 11-(ethylamino)undecanoic acid may vary depending on its purity and the presence of any impurities or additives.
Boiling point
Varies depending on the specific compound The boiling point of 11-(ethylamino)undecanoic acid may also vary depending on its purity and the presence of any impurities or additives.
Density
Varies depending on the specific compound The density of 11-(ethylamino)undecanoic acid may vary depending on its molecular weight and the presence of any impurities or additives.
Reactivity
Reacts with acids, bases, and other functional groups As a carboxylic acid and an amino acid derivative, it can react with acids, bases, and other functional groups to form various products.
Check Digit Verification of cas no
The CAS Registry Mumber 7441-35-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7441-35:
(6*7)+(5*4)+(4*4)+(3*1)+(2*3)+(1*5)=92
92 % 10 = 2
So 7441-35-2 is a valid CAS Registry Number.
7441-35-2Relevant academic research and scientific papers
Polyanion inhibitors of human immunodeficiency virus and other viruses. 5. Telomerized anionic surfactants derived from amino acids
Leydet, Alain,Barragan, Véronique,Boyer, Bernard,Montéro, Jean Louis,Roque, Jean Pierre,Witvrouw, Myriam,Este, José,Snoeck, Robert,Andrei, Graciela,De Clercq, Erick
, p. 342 - 349 (2007/10/03)
ω-Acryloyl anionic surfactants, whose polar heads are derived from amino acids, have been telomerized to prepare polyanions of a predetermined molecular weight. The main goal of this study was to verify whether the antiviral activity is influenced by the degree of polymerization of the polyanions. The oligomeric polyanions were evaluated for their activity against human immunodeficiency virus (HIV-1 or HIV-2) and various other RNA and DNA viruses. With regard to their anti-HIV activity, a minimum number of anionic groups was necessary to achieve an inhibitory effect. Moreover, to be active the overall conformation of the polyanion must be such that the anionic groups are located on the external site of the molecule. With some of the polyanions, a 50% inhibition concentration (IC50) as low as 1 μg/mL, or even 0.1 μg/mL, was noted against HIV-1 in CEM-4 and MT-4 cells, respectively. The most potent polyanions also proved active against human cytomegalovirus and herpex simplex virus at concentrations of 5-10 and 20-40 μg/mL, respectively. No activity was observed against any of the other viruses tested (i.e., vesicular stomatitis, Sindbis, Semliki forest, parainfluenza, Junin, Tacaribe, Coxsackie, polio, reo, and vaccinia). No toxicity for the host cells was observed at concentrations up to 200 μg/mL.
