2-{[Bis(2-chloroethyl)amino]methyl}-L-phenylalanine, with the CAS number 2185-98-0, is a synthetic amino acid derivative that exhibits characteristics typical of both amino acids and alkylating agents. This compound features a phenylalanine backbone, which is an essential amino acid known for its role in protein synthesis and neurotransmitter production. The presence of the bis(2-chloroethyl)amino group indicates that it has potential reactivity, particularly in biological systems, where it may act as an alkylating agent, potentially leading to DNA cross-linking. This property is of interest in medicinal chemistry, particularly in the development of chemotherapeutic agents. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its structure suggests that it could interact with biological macromolecules, influencing cellular processes. Safety considerations are important due to the presence of chlorine atoms, which can pose toxicity risks. Overall, this compound represents a unique intersection of amino acid functionality and alkylating reactivity, making it a subject of interest in both research and therapeutic contexts.

2-{[bis(2-chloroethyl)amino]methyl}-L-phenylalanine

2185-98-0: 2-{[Bis(2-chloroethyl)amino]methyl}-L-phenylalanine, with the CAS number 2185-98-0, is a synthetic amino acid derivative that exhibits characteristics typical of both amino acids and alkylating agents. This compound features a phenylalanine backbone, which is an essential amino acid known for its role in protein synthesis and neurotransmitter production. The presence of the bis(2-chloroethyl)amino group indicates that it has potential reactivity, particularly in biological systems, where it may act as an alkylating agent, potentially leading to DNA cross-linking. This property is of interest in medicinal chemistry, particularly in the development of chemotherapeutic agents. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its structure suggests that it could interact with biological macromolecules, influencing cellular processes. Safety considerations are important due to the presence of chlorine atoms, which can pose toxicity risks. Overall, this compound represents a unique intersection of amino acid functionality and alkylating reactivity, making it a subject of interest in both research and therapeutic contexts.

<p>Ocaphane Hydrochloride is a strong antitumor agent used on a number of animal tumors.</p>

CAS 2185-98-0

2-{[bis(2-chloroethyl)amino]methyl}-L-phenylalanine

Ocaphane Hydrochloride

Ref: TM-T26365L