13726-16-4

Basic information

• Product Name: 3-CHLORO-4-METHOXYBENZALDEHYDE
• Synonyms: TIMTEC-BB SBB003854;3-CHLORO-4-METHOXYBENZALDEHYDE;3-CHLORO-4-METHOXYBENZENECARBALDEHYDE;3-CHLORO-P-ANISALDEHYDE;AKOS B029259;CHEMBRDG-BB 6945816;3-Methoxy-4-chlorobenzaldehyde
• CAS NO: 13726-16-4
• Molecular Formula: C₈H₇ClO₂
• Molecular Weight: 170.59
• Mol File: 13726-16-4.mol
• Article Data: 14

Chemical Properties

• Melting Point: 56-60 °C(lit.)
• Boiling Point: 265℃
• Flash Point: 118℃
• Appearance: White to pale brown/Powder
• Density: 1.244
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 3-CHLORO-4-METHOXYBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLORO-4-METHOXYBENZALDEHYDE(13726-16-4)
• EPA Substance Registry System: 3-CHLORO-4-METHOXYBENZALDEHYDE(13726-16-4)

Safety Data

• Hazard Codes: Xi
• Safety Statements: 22-24/25
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 13726-16-4(Hazardous Substances Data)

Usage

General Description

3-Chloro-4-Methoxybenzaldehyde is an organic compound with the chemical formula C8H7ClO2. It is a white to light yellow crystalline powder that is commonly used in the synthesis of pharmaceuticals and other organic compounds. This chemical is known for its aromatic and aldehyde properties, making it useful in the production of fragrances and flavors. It is also used in the manufacture of agrochemicals and dyes. 3-Chloro-4-Methoxybenzaldehyde is considered to be a versatile building block in organic chemistry and is widely used in the pharmaceutical and chemical industries for its various applications.

Upstream product

• 75-17-2 formaldoxime 
• 13726-14-2 4-chloro-m-anisidine 
• 67-56-1 methanol 
• 104-88-1 4-chlorobenzaldehyde 
• 189942-81-2 1-chloro-4-dichloromethyl-2-methoxy-benzene 
• 75-89-8 2,2,2-trifluoroethanol 
• 97-52-9 2-methoxy-4-nitrophenylamine 
• 1009-36-5 2-chloro-5-nitroanisole 
• 615-74-7 2-chloro-5-methylphenol 
• 73909-16-7 2-chloro-5-methylanisole 
• 13726-17-5 (4-chloro-3-methoxyphenyl)methan-1-ol 
• 56962-12-0 3-hydroxy-4-chlorobenzaldehyde 
• 77-78-1 dimethyl sulfate 
• 16817-43-9 5-Bromo-2-chloroanisole 

Downstream Products

• 96495-22-6 2-(4-chloro-3-methoxyphenyl)ethylamine 
• 144181-29-3 N-propionyl-2-(4-chloro-3-methoxyphenyl)ethylamine 
• 144181-30-6 N-(phenylacetyl)-2-(4-chloro-3-methoxyphenyl)ethylamine 
• 144181-31-7 N-<(3-methoxyphenyl)acetyl>-2-(4-chloro-3-methoxyphenyl)ethylamine 
• 144181-32-8 N-<(4-methoxyphenyl)acetyl>-2-(4-chloro-3-methoxyphenyl)ethylamine 
• 144181-33-9 N-<3-(4-methoxyphenyl)propionyl>-2-(4-chloro-3-methoxyphenyl)ethylamine 
• 1365763-71-8 ethyl 4-chloro-3-methoxyphenethylcarbamate 
• 1207549-31-2 C₁₉H₁₉ClN₂O₅ 
• 116022-18-5 methyl 4-chloro-3-methoxybenzoate 
• 73898-63-2 1-(4-chloro-3-methoxyphenyl)ethan-1-one 

Relevant articles and documents

PLATELET ADP RECEPTOR INHIBITORS

no abstract published

Electrochemical methoxylation of some benzaldehyde derivatives at platinum electrode

The electrochemical methoxylation of 4-chlorobenzaldehyde, 4-hydroxybenzatdehyde, 4-anisylaldehyde and 4,4-N,N′- dimethylaminobenzaldehyde was carried out at platinum electrode. Constant potential electrolysis was carried out in undivided electrochemical cell. The reaction is an example of nuclear oxidation of aromatic compounds with substitution. The experimental parameters involved in the reaction are discussed here.

Intermediate compounds and methods for synthesizing chemiluminescent dioxetane substrates

Methods for synthesizing 1,2-dioxetane compounds and intermediate compounds useful in the synthesis of these dioxetane compounds are described. The methods and intermediates allow for the efficient production of dioxetane substrates having electron withdr