153842-00-3

Basic information

• Product Name: N-(Chloroacetyl)-alanine Methyl Ester
• Synonyms: N-(Chloroacetyl)-alanine Methyl Ester;N-(Chloroacetyl)-DL-alanine Methyl Ester
• CAS NO: 153842-00-3
• Molecular Formula: C6H10ClNO3
• Molecular Weight: 179.6015
• Product Categories: Amino Acids & Derivatives;MTS & Sulfhydryl Active Reagents;Amino Acids & Derivatives, MTS & Sulfhydryl Active Reagents
• Mol File: 153842-00-3.mol

Chemical Properties

• Boiling Point: 288.0±20.0 °C(Predicted)
• Appearance: /
• Density: 1 +-.0.06 g/cm3(Predicted)
• Solubility: Benzene
• PKA: 12.56±0.46(Predicted)
• CAS DataBase Reference: N-(Chloroacetyl)-alanine Methyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(Chloroacetyl)-alanine Methyl Ester(153842-00-3)
• EPA Substance Registry System: N-(Chloroacetyl)-alanine Methyl Ester(153842-00-3)

Safety Data

• Hazardous Substances Data: 153842-00-3(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
N-(Chloroacetyl)-alanine Methyl Ester is used as a synthetic building block for the creation of various complex organic molecules. Its unique structure allows it to be a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-(Chloroacetyl)-alanine Methyl Ester is used as an intermediate in the development of new drugs. Its reactivity and functional groups make it a valuable compound for the synthesis of biologically active molecules with potential therapeutic applications.
Used in Agrochemical Industry:
N-(Chloroacetyl)-alanine Methyl Ester is also utilized in the agrochemical industry for the synthesis of compounds with pesticidal, herbicidal, or fungicidal properties. Its incorporation into these molecules can enhance their effectiveness and selectivity in controlling pests and diseases in agriculture.
Used in Research and Development:
In the field of research and development, N-(Chloroacetyl)-alanine Methyl Ester serves as a key compound for exploring new reaction pathways and understanding the fundamental chemistry of amino acid derivatives. This knowledge can be applied to the design and synthesis of novel molecules with specific properties and applications.