CAS 1124-40-9
:1,2-Benzenediol, 4-(aminomethyl)-, hydrochloride (1:1)
Description:
1,2-Benzenediol, 4-(aminomethyl)-, hydrochloride (1:1), commonly known as 4-(aminomethyl)catechol hydrochloride, is an organic compound characterized by its aromatic structure featuring a catechol moiety with an amino group attached to the benzene ring. This compound appears as a white to off-white crystalline solid and is soluble in water due to the presence of the hydrochloride salt, which enhances its solubility compared to the free base form. It exhibits properties typical of both phenolic and amine functionalities, making it a versatile intermediate in organic synthesis. The amino group can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, while the catechol structure can engage in redox reactions and complexation with metal ions. This compound is often utilized in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, owing to its reactivity and functional versatility. Safety data should be consulted for handling, as with many chemical substances, it may pose health risks if not managed properly.
Formula:C7H9NO2·ClH
InChI:InChI=1S/C7H9NO2.ClH/c8-4-5-1-2-6(9)7(10)3-5;/h1-3,9-10H,4,8H2;1H
InChI key:InChIKey=LFRARYNEDYNCOT-UHFFFAOYSA-N
SMILES:C(N)C1=CC(O)=C(O)C=C1.Cl
Synonyms:- 3,4-Dihydroxybenzylamine hydrochloride
- 1,2-Benzenediol, 4-(aminomethyl)-, hydrochloride
- Pyrocatechol, 4-(aminomethyl)-, hydrochloride
- 1,2-Benzenediol, 4-(aminomethyl)-, hydrochloride (1:1)
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Found 1 products.
4-(Aminomethyl)-1,2-benzenediol hydrochloride
CAS:<p>4-(Aminomethyl)-1,2-benzenediol hydrochloride is a potent inhibitor of monoamine neurotransmitter synthesis. It has been shown to inhibit the polymerase chain reaction (PCR) and is effective in the preparation of samples for PCR analysis. 4-(Aminomethyl)-1,2-benzenediol hydrochloride is chemically stable and has an electrochemical detector that can be used in its detection. This chemical also inhibits the incorporation of thymidine into DNA during DNA synthesis, leading to a decrease in DNA synthesis. The monoclonal antibody technique has been used to detect this compound in human serum and tissue biopsies.</p>Formula:C7H10ClNO2Purity:Min. 95%Molecular weight:175.61 g/mol
