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What is an amine Nitrogen-containing group with a nutrient chemical structure?
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∙ 10y ago
amino acide
Wiki User
∙ 10y ago
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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 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 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 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 structural formula for the compound amine?
The structural formula for a generic amine compound can be represented as R-NH2, where R represents a substituent group. Amines are organic compounds containing a nitrogen atom bonded to one or more alkyl or aryl groups.
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.
What is an aminoketone?
An aminoketone is a chemical compound containing both a ketone group and an amine.
What is amine swetenning of natural gas?
Amine sweetening is a process used to remove acidic gases, such as hydrogen sulfide and carbon dioxide, from natural gas. This is achieved by bringing the natural gas in contact with a solution of amine compounds, which selectively absorb the acidic gases. After the amine solution absorbs the acidic gases, it is regenerated to release the gases and be reused in the process.
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.
Is there any amino acid having secondary amino group in its structure?
The amino acid proline is the only amino acid that has a secondary amine functional group. This is because proline is a cyclic amino acid that links the 3-carbon R-group back to the amine group, resulting in a secondary amine.
