1201-91-8

Basic information

• Product Name: N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde
• Synonyms: 4-(N-METHYL-N-HYDROXYETHYL)AMINOBENZALDEHYDE;N-Methyl-N-Hydroxyethyl-p-Amino Benzaldehyde;N-METHYL-N-(2-HYDROXYETHYL)-4-AMINOBENZA;p-(N-2-hydroxyethyl-N-methyl)aminobenzaldehyde;N-Methyl-N-(2-hydrox;N-Methyl-N-ethoxyl-4-aMino benzaldehyde;N-Methyl-N-(2-hydroxyethyl)-4-aMinobenzaldehyde 96%;N-METHYL-N-(2-HYDROXYETHYL)-4-AMINOBENZALDEHYDE
• CAS NO: 1201-91-8
• Molecular Formula: C₁₀H₁₃NO₂
• Molecular Weight: 179.22
• Product Categories: Intermediates of Dyes and Pigments;Aldehydes;C10 to C21;Carbonyl Compounds
• Mol File: 1201-91-8.mol
• Article Data: 13

Chemical Properties

• Melting Point: 66-70 °C(lit.)
• Boiling Point: 354.037 °C at 760 mmHg
• Flash Point: 167.916 °C
• Appearance: Light yellow powder
• Density: 1.171 g/cm³
• Vapor Pressure: 1.27E-05mmHg at 25°C
• Refractive Index: 1.615
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 14.58±0.10(Predicted)
• CAS DataBase Reference: N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde(1201-91-8)
• EPA Substance Registry System: N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde(1201-91-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 1201-91-8(Hazardous Substances Data)

Usage

Description

N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde is an organic compound with the chemical formula C10H13NO2. It is a derivative of benzaldehyde, featuring a methyl group, a 2-hydroxyethyl group, and an amino group attached to the benzene ring. N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde is known for its potential applications in various chemical and material synthesis processes.

Uses

Used in Optical Materials Synthesis:
N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde is used as a key intermediate in the synthesis of crosslinkable tricyanopyrroline polymeric electro-optic materials. These materials exhibit high nonlinear optical properties and are crucial for the development of advanced photonic devices and communication systems.
Used in Polymer Synthesis:
N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde is also utilized in the chemical process for synthesizing polymethacrylates, which are a class of polymers with diverse applications, including coatings, adhesives, and dental materials.
Used in Organic Synthesis:
N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde may be used to synthesize various organic compounds, such as:
1. 2,5-bis[4-(methylaminoethanol)benzylidene]cyclopentanone: N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde can be used as a precursor in the synthesis of complex organic molecules or as a building block in material science.
2. 4′-[(Tosyloxyethyl)(methyl)amino]-4-phenyl-3-buten-2-malonitrile: A tosylate precursor that can be employed in the synthesis of pharmaceuticals or other organic compounds.
3. Methanesulfonic acid 2-[(4-formyl-phenyl)-methyl-amino]-ethyl ester: This ester can be used as an intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

InChI:InChI=1/C10H13NO2/c1-11(6-7-12)10-4-2-9(8-13)3-5-10/h2-5,8,12H,6-7H2,1H3

Upstream product

• 94-31-5 N-(2-chloroethyl)-N-methyl-4-aminobenzaldehyde 
• 19520-89-9 2-(methyl(phenyl)amino)ethyl acetate 
• 68-12-2 N,N-dimethyl-formamide 
• 50-00-0 formaldehyd 
• 93-90-3 N-(2-hydroxyethyl)-N-methylaminobenzene 
• 109-83-1 (2-hydroxyethyl)(methyl)amine 
• 459-57-4 4-fluorobenzaldehyde 
• 1669-85-8 N-(2-chloroethyl)-N-methylaniline 

Downstream Products

• 161465-10-7 N-(2-hydroxyethyl)-N-methyl-4-(1-hydroxy-2-phenylethyl)aniline 
• 736981-11-6 2-[4-formyl(methyl)anilino]ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate 
• 942412-60-4 C₁₃H₁₉NO₅S 

Relevant articles and documents

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