Product Description
| 2-氯-4-氨基苯甲酸甲酯(固体) |
Methyl 2-chloro-4-aminobenzoate |
| CAS RN |
46004-37-9 |
| Purity / Analysis Method |
>99.0%(GC) |
| Molecular Formula / Molecular Weight |
C8H8ClNO2 = 185.61 |
| Physical State (20 deg.C) |
Solid |
| Storage Temperature |
Room Temperature (Recommended in a cool and dark place, <15°C) |
| Appearance |
White to Almost white powder to crystal |
| Melting point |
108.0 to 112.0 °C |
AI Product Description
*The following content is generated by AI and is for reference only.
Methyl 2-chloro-4-aminobenzoate is a specialized organic intermediate widely utilized in the pharmaceutical and agrochemical industries. With the Chemical Abstracts Service (CAS) number 17935-68-3, this compound features a benzene ring substituted with a methyl ester group at the first position, a chlorine atom at the second position, and an amino group at the fourth position. Its molecular formula is C8H8ClNO2, and it possesses a molar mass of approximately 185.61 g/mol. The molecule typically appears as a yellow to brown crystalline powder or solid, characterized by moderate solubility in common organic solvents such as ethanol, ethyl acetate, and dichloromethane, while remaining largely insoluble in water.
The primary application of Methyl 2-chloro-4-aminobenzoate lies in its role as a key building block for synthesizing complex heterocyclic compounds and active pharmaceutical ingredients (APIs). It serves as a crucial precursor in the production of various sulfonamide derivatives and other nitrogen-containing heterocycles that exhibit significant biological activity. In the pharmaceutical sector, intermediates derived from this compound are often investigated for their potential anti-inflammatory, antimicrobial, and analgesic properties. Furthermore, the presence of both the chloro and amino functionalities allows for versatile chemical modifications, including nucleophilic substitution reactions and coupling processes, making it highly valuable for medicinal chemists designing novel drug candidates.
In the agrochemical field, this substance contributes to the synthesis of specific herbicides and fungicides. The structural integrity provided by the chloro-amino-benzoate scaffold enables the development of compounds that effectively target plant pathogens or weed growth mechanisms. Due to its reactivity, handling requires standard laboratory safety precautions, including the use of personal protective equipment to avoid skin contact or inhalation of dust. Overall, Methyl 2-chloro-4-aminobenzoate remains an essential component in modern chemical manufacturing, bridging the gap between basic organic chemistry and advanced therapeutic or agricultural applications. Its availability supports ongoing research into new bioactive molecules, driving innovation across multiple scientific disciplines.