CAS 6288-63-7
:N-(2-chloroethyl)benzylamine hydrochloride
Description:
N-(2-chloroethyl)benzylamine hydrochloride is an organic compound characterized by its amine functional group and a chloroethyl substituent. It appears as a white to off-white crystalline solid and is soluble in water, which is typical for many hydrochloride salts. The compound features a benzyl group attached to a nitrogen atom, which is further substituted with a 2-chloroethyl group, contributing to its reactivity and potential applications in medicinal chemistry. As a hydrochloride salt, it is often more stable and easier to handle than its free base form. This compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of agents targeting specific receptors or pathways. However, due to the presence of the chloroethyl moiety, it may also pose certain safety and handling considerations, as chloroalkyl groups can be associated with alkylating activity. Proper safety protocols should be followed when working with this substance in a laboratory setting.
Formula:C9H12ClN
InChI:InChI=1/C9H12ClN/c10-6-7-11-8-9-4-2-1-3-5-9/h1-5,11H,6-8H2
InChI key:InChIKey=RAJZCNAPSJZGBF-UHFFFAOYSA-N
SMILES:C(NCCCl)C1=CC=CC=C1.Cl
Synonyms:- 2-Chloro-N-(phenylmethyl)ethanamine hydrochloride
- Benzenemethanamine, N-(2-chloroethyl)-, hydrochloride
- Benzenemethanamine, N-(2-chloroethyl)-, hydrochloride (1:1)
- Benzenemethanamine, N-(2-chloroethyl)-, hydrochloride (9CI)
- Benzylamine, N-(2-chloroethyl)-, hydrochloride
- N-Benzyl-N-(2-chloroethyl)amine hydrochloride
- N-Benzyl-N-(2-chloroethyl)ammonium chloride
- N-benzyl-2-chloroethanamine
- N-benzyl-2-chloroethanaminium chloride
- Nsc 11462
- N-(2-Chloroethyl)benzylamine hydrochloride
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
N-Benzyl-N-(2-chloroethyl)amine hydrochloride
CAS:Formula:C9H13Cl2NPurity:97.0%Color and Shape:SolidMolecular weight:206.11N-Benzyl-N-(2-chloroethyl)amine hydrochloride
CAS:<p>N-Benzyl-N-(2-chloroethyl)amine hydrochloride is an aniline derivative that is catalytically converted to an isocyanate. It has been used as a chiral building block for the synthesis of analogues and can be used in high yield as a regiospecific sulfone formation. The chlorosulfonyl chloride is generated in situ from triethylamine and chlorosulfonyl isocyanate, which leads to cyclic sulfones.</p>Formula:C9H13Cl2NPurity:Min. 95%Molecular weight:206.11 g/mol


