172217-11-7

Basic information

• Product Name: ETHYL 2-AMINO-6-CHLOROBENZOATE
• Synonyms: ETHYL 2-AMINO-6-CHLOROBENZOATE
• CAS NO: 172217-11-7
• Molecular Formula: C₉H₁₀ClNO₂
• Molecular Weight: 199.63
• Mol File: 172217-11-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: ETHYL 2-AMINO-6-CHLOROBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2-AMINO-6-CHLOROBENZOATE(172217-11-7)
• EPA Substance Registry System: ETHYL 2-AMINO-6-CHLOROBENZOATE(172217-11-7)

Safety Data

• Hazardous Substances Data: 172217-11-7(Hazardous Substances Data)

Usage

General Description

Ethyl 2-amino-6-chlorobenzoate is a chemical compound with the molecular formula C9H10ClNO2. It is an organic compound that belongs to the class of benzoic acids and derivatives. This chemical is a white crystalline solid that is often used as an intermediate in the production of various pharmaceuticals and agrochemicals. It has also shown potential as a building block in the synthesis of bioactive molecules. Ethyl 2-amino-6-chlorobenzoate is known for its wide range of applications in the field of medicinal chemistry and pharmaceutical research, making it an important compound in the chemical industry.

Upstream product

• 64-17-5 ethanol 
• 2148-56-3 2-chloro-6-aminobenzoic acid 
• 141-52-6 sodium ethanolate 
• 75-03-6 ethyl iodide 
• 172217-16-2 ethyl 2-chloro-6-nitrobenzoate 

Downstream Products

• 112270-06-1 ethyl 2-chloro-6-hydroxybenzoate 
• 172217-13-9 ethyl 6-chloro-2-methoxycarbanilate 
• 172217-12-8 ethyl 6-chloro-2-methoxybenzoate 
• 3260-89-7 2-chloro-6-methoxybenzoic acid 
• 379230-45-2 3-allyl-6-chloro-2-hydroxybenzoate 
• 412349-25-8 2-(4-chloro-3-ethoxycarbonyl-2-hydroxyphenyl)acetaldehyde 
• 379230-44-1 ethyl 2-(allyloxy)-6-chlorobenzoate 
• 379230-47-4 6-chloro-1-benzofuran-7-carboxylic acid 
• 379230-43-0 6-chloro-1-benzofuran-7-amine 

Relevant articles and documents

AMPK MODULATORS

The present invention relates to compounds and pharmaceutically acceptable salts, esters and prodrugs of Formula (I) or (II), which are useful as AMPK modulators effective in treating diabetes, obesity and cancer in a subject.

QUINAZOLINE DERIVATIVES FOR THE TREATMENT OF TUMOURS

The invention concerns quinazoline derivatives of Formula (I) wherein each of Q1, Z, m, R1, R2, R3 and Q2 have any of the meanings defined in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an anti-invasive agent in the containment and/or treatment of solid tumour disease

Fischer indolization of ethyl pyruvate 2-bis(2-methoxyphenyl)hydrazone and new insight into the mechanism of Fischer indolization. (Fischer indolization and its related compounds. XXVII)

In connection with studies on the direction of cyclization in the Fischer indolization of substituted diphenylhydrazones, the Fischer indolization of ethyl pyruvate 2-bis(2-methoxyphenyl)hydrazone (6) was carried out. The result showed that cyclization in Fischer indolization of diphenylhydrazone does not always proceed to the electron-richer nucleus, but depends on the conformation of the enehydrazine. Thus, the Fischer indolization should proceed via a [3,3] sigmatropic route, with an electronic effect.