0
Add your answer:
Earn +20 pts
Chemical structure of hexamethylene di amine?
The chemical structure of hexamethylene diamine is H2N-(CH2)6-NH2. It is a linear aliphatic diamine consisting of a six-carbon chain with an amino group at each end.
What is the chemical reaction for furfural and a primary aromatic amine C5H4O2 plus Nh2?
The chemical reaction between furfural (C5H4O2) and a primary aromatic amine (C5H4NH2) typically results in the formation of a Schiff base compound. This reaction involves the condensation of the carbonyl group of furfural with the primary amine group of the aromatic amine, leading to the formation of an imine linkage. The reaction is generally carried out in the presence of a suitable catalyst under mild conditions.
What is an aminoketone?
An aminoketone is a chemical compound containing both a ketone group and an amine.
What is the chemical make up in Strattera?
The chemical name is very long: (3R)-N-methyl-3-(2-methylphenoxy)-3-phenylpropan-1-amine; (R)-N-methyl-3-phenyl-3-(o-tolyloxy)propan-1-amine.
Are oils considered amino acids?
Oils are not amine acids. Oils do not have NH2 and COOH groups in their structure.
What is the chemical structure of 2-methylpropan-2-amine and how is it used in pharmaceuticals?
The chemical structure of 2-methylpropan-2-amine is C4H11N. It is used in pharmaceuticals as a precursor in the synthesis of various drugs, including certain antidepressants and stimulants.
What is the secondary amine with the molecular formula C3H9N?
The secondary amine with the molecular formula C3H9N is dimethylamine. It has the chemical structure CH3-NH-CH3, with two methyl groups attached to the nitrogen atom.
Chemical structure of hexamethylene di amine?
The chemical structure of hexamethylene diamine is H2N-(CH2)6-NH2. It is a linear aliphatic diamine consisting of a six-carbon chain with an amino group at each end.
What is the chemical name for C5H5N5?
It is the chemical formula for any one of these= Adenine (or 9H-purin-6-amine)= 2-Aminopurine (or 7H-purin-2-amine)
What compromises a protein in a primary structure?
There are over 300 amine acids found in nature. Out of these only 20 are found in human body. One amine acid is attached to other by pep-tide bond and there is chain of amine acids and it makes the primary structure of proteins.
What is the chemical reaction for furfural and a primary aromatic amine C5H4O2 plus Nh2?
The chemical reaction between furfural (C5H4O2) and a primary aromatic amine (C5H4NH2) typically results in the formation of a Schiff base compound. This reaction involves the condensation of the carbonyl group of furfural with the primary amine group of the aromatic amine, leading to the formation of an imine linkage. The reaction is generally carried out in the presence of a suitable catalyst under mild conditions.
Mdma chemical structure?
The chemical structure of MDMA, or 3,4-methylenedioxy-N-methylamphetamine, consists of a phenethylamine core with a methylenedioxy ring substitution at the 3 and 4 positions. It also contains a methyl group bound to the terminal amine nitrogen.
What is ch3ch2nch2ch3?
This is the chemical formula for diethylamine, which is a secondary amine. It is a colorless liquid with a fishy odor, commonly used as a solvent and in organic synthesis.
Does amine act as a base in chemical reactions?
Yes, amines can act as bases in chemical reactions by accepting protons.
What is an aminoketone?
An aminoketone is a chemical compound containing both a ketone group and an amine.
What is the key difference between an amine and an amide in terms of their chemical structures and properties?
The key difference between an amine and an amide is in their chemical structure. Amines have a nitrogen atom bonded to one or more carbon atoms, while amides have a nitrogen atom bonded to a carbonyl group (CO). This structural difference leads to differences in their properties, with amines typically being more basic and amides being more stable and less basic.
What is the chemical make up in Strattera?
The chemical name is very long: (3R)-N-methyl-3-(2-methylphenoxy)-3-phenylpropan-1-amine; (R)-N-methyl-3-phenyl-3-(o-tolyloxy)propan-1-amine.
