158966-62-2

Basic information

• Product Name: 2-Chloro-6-methoxyaniline
• Synonyms: 2-Chloro-6-methoxyaniline
• CAS NO: 158966-62-2
• Molecular Formula: C₇H₈ClNO
• Molecular Weight: 157.59752
• Mol File: 158966-62-2.mol

Chemical Properties

• Boiling Point: 246 °C
• Appearance: /
• Density: 1.234±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 2.60±0.10(Predicted)
• CAS DataBase Reference: 2-Chloro-6-methoxyaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Chloro-6-methoxyaniline(158966-62-2)
• EPA Substance Registry System: 2-Chloro-6-methoxyaniline(158966-62-2)

Safety Data

• Hazardous Substances Data: 158966-62-2(Hazardous Substances Data)

Usage

Uses

Used in Dye Production:
2-Chloro-6-methoxyaniline is used as a chemical intermediate for the synthesis of various dyes. Its unique chemical structure allows for the creation of a wide range of colors, making it a valuable component in the dye industry.
Used in Pharmaceutical Industry:
2-Chloro-6-methoxyaniline is used as a building block in the synthesis of certain pharmaceutical compounds. Its presence in the molecular structure can contribute to the development of new drugs with potential therapeutic applications.
Used in Rubber Industry:
2-Chloro-6-methoxyaniline is used as a component in the production of rubber, where it may contribute to the modification of rubber properties, such as improving its durability or flexibility.
Used in Laboratory Research:
2-Chloro-6-methoxyaniline is used as a research chemical in various laboratory experiments. Its reactivity and properties make it a useful tool for studying chemical reactions and processes in the field of organic chemistry.

Upstream product

• 5472-99-1 3-chloro-2-nitroanisole 
• 578-57-4 2-bromoanisole 
• 172217-13-9 ethyl 6-chloro-2-methoxycarbanilate 
• 64-19-7 acetic acid 
• 4920-80-3 3-methoxy-2-nitrobenzoic acid 
• 16554-47-5 3-methoxy-2-nitroaniline 
• 15865-57-3 2-nitro-3-methoxybenzoyl chloride 
• 119-81-3 4-methoxy-2-nitroacetanilide 
• 5473-00-7 4-methoxy-2,3-dinitro-aniline 
• 62153-30-4 acetic acid-(4-methoxy-2,3-dinitro-anilide) 
• 51-66-1 4-methoxyacetanilide 
• 934537-35-6 N-(2-chloro-6-methoxyphenyl)-2,2-dimethylpropionamide 

Downstream Products

• 6575-10-6 2-Chlor-6-methoxybenzoesaeurenitril 
• 174913-08-7 2-bromo-3-chloro-anisole 
• 791642-67-6 1-chloro-2-iodo-3-methoxybenzene 
• 723324-78-5 2-chloro-4-iodo-6-methoxy-aniline 
• 82344-35-2 N-aceto-2-chloro-6-methoxyaniline 
• 116571-70-1 chloro-acetic acid-(2-chloro-6-methoxy-anilide) 
• 70630-34-1 2-[(2-Chloro-6-methoxy-phenyl)-(2-methoxy-acetyl)-amino]-propionic acid methyl ester 
• 158966-64-4 1-(2-Chloro-6-methoxy-phenyl)-1H-pyrrole 
• 1027526-40-4 1-(2-Chloro-6-methoxy-phenyl)-3-pentyl-urea 
• 158966-68-8 3-Chloro-1-(2-chloro-6-methoxy-phenyl)-1H-pyrrole 
• 158966-67-7 2-Chloro-1-(2-chloro-6-methoxy-phenyl)-1H-pyrrole 
• 158966-75-7 1-(2-Chloro-6-methoxy-phenyl)-1H-pyrrole-2-carboxylic acid 
• 148726-42-5 1-(2-Chloro-6-hydroxy-phenyl)-3-pentyl-urea 
• 99585-06-5 acetic acid-(2-chloro-6-methoxy-4-nitro-anilide) 

Relevant articles and documents

BENZOXAZOLES USEFUL IN THE TREATMENT OF INFLAMMATION

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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.

Structure-activity relationship of a series of phenylureas linked to 4- phenylimidazole. Novel potent inhibitors of acyl-CoA:cholesterol O- acyltransferase with antiatherosclerotic activity. 2

In our continuing search to find systemically bioavailable ACAT (acyl- CoA:cholesterol O-acyl-transferase) inhibitors with more potent antiatherosclerotic effect than N-[2-(dimethylamino)-6-[3-(5-methyl-4- phenyl-1H-imidazol-1-yl)propoxy]phenyl]-N'-pentyl