35708-19-1

Basic information

• Product Name: 2-Anilinobenzoic acid methyl ester
• Synonyms: 2-(Phenylamino)benzoic acid methyl ester;2-Anilinobenzoic acid methyl ester;Benzoic acid, 2-(phenylaMino)-, Methyl ester;methyl 2-(phenylamino)benzoate
• CAS NO: 35708-19-1
• Molecular Formula: C₁₄H₁₃NO₂
• Molecular Weight: 227.26
• Mol File: 35708-19-1.mol
• Article Data: 52

Chemical Properties

• Melting Point: 58-59 °C
• Boiling Point: 140 °C(Press: 0.1 Torr)
• Appearance: /
• Density: 1.175±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: -1.27±0.20(Predicted)
• CAS DataBase Reference: 2-Anilinobenzoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Anilinobenzoic acid methyl ester(35708-19-1)
• EPA Substance Registry System: 2-Anilinobenzoic acid methyl ester(35708-19-1)

Safety Data

• Hazardous Substances Data: 35708-19-1(Hazardous Substances Data)

Usage

General Description

2-Anilinobenzoic acid methyl ester is a chemical compound with the molecular formula C14H13NO2. It is an ester derivative of benzoic acid, with a methyl group attached to the carboxyl group. The anilino group, consisting of an aniline ring with a benzene ring attached, is also present in the molecule. This chemical is commonly used in organic synthesis and pharmaceutical research as a building block for the preparation of various pharmaceutical compounds and dyes. It is also utilized in the production of fragrances and other industrial applications. Due to its various uses and applications, 2-Anilinobenzoic acid methyl ester is an important intermediate in the chemical industry.

Upstream product

• 67-56-1 methanol 
• 91-40-7 2-(phenylamino)benzoic acid 
• 77-78-1 dimethyl sulfate 
• 19263-30-0 3-phenyl-1,2,3-benzotriazin-4(3H)-one 
• 591-50-4 iodobenzene 
• 134-20-3 2-carbomethoxyaniline 
• 62-53-3 aniline 
• 278175-48-7 methyl 2-(perfluoro-1-butanesulfonyloxy)benzoate 
• 117560-06-2 3-phenyliodonio-1,2,4-trioxo-1,2,3,4-tetrahydronaphthalenide 
• 108-86-1 bromobenzene 
• 74-88-4 methyl iodide 
• 119-36-8 methyl salicylate 
• 12775-96-1 copper 
• 610-94-6 2-bromobenzoic acid methyl ester 

Downstream Products

• 412017-59-5 3-[2-(phenylamino)phenyl]pentan-3-ol 
• 168558-34-7 2-(tert-butyl)-N-phenylaniline 
• 230627-85-7 diphenyl(2-(phenylamino)phenyl)methanol 
• 87485-99-2 Methyl 5-bromo-N-(2',4'-dibromophenyl)anthranilate 
• 1211-19-4 2-phenylaminobenzamide 
• 23857-21-8 2-methoxy-1-phenyl-2-thioxo-1,2-dihydro-2λ⁵-benzo[d][1,3,2]thiazaphosphinine-4-thione 
• 99233-97-3 2-<(2-Acetylphenyl)phenylamino>benzoesaeure-methylester 
• 73183-49-0 2-<(2-Benzoylphenyl)phenylamino>benzoesaeure-methylester 
• 76681-81-7 1-phenyl-3-methyl-2,4-(1H,3H)quinazolinedione 
• 91855-59-3 N-Chloracetyl-N-phenylanthranilsaeuremethylester 
• 146828-49-1 N-phenyl-2-carbomethoxymalonanilic acid ethyl ester 
• 49604-61-7 N-methyl-2-(phenylamino)benzamide 
• 20877-86-5 N-phenyl isatoic anhydride 
• 57623-78-6 N-(4-methoxyphenyl)-2-(phenylamino)benzamide 

Relevant articles and documents

Bridging Small Molecules to Conjugated Polymers: Efficient Thermally Activated Delayed Fluorescence with a Methyl-Substituted Phenylene Linker

Based on a “TADF + Linker” strategy (TADF=thermally activated delayed fluorescence), demonstrated here is the successful construction of conjugated polymers that allow highly efficient delayed fluorescence. Small molecular TADF blocks are linked together

Dark blue electroluminescent compound and preparation method and application thereof

The invention discloses a dark blue electroluminescent compound and a preparation method and application thereof, and the compound is 2-(4-(9, 9-dimethylacridin-10(9H)-yl)-2, 5-diR2-based phenyl)-1-(4-R1-based phenyl)-1H-phenanthroimidazole. The preparation method of the compound is easy to operate and high in yield, the compounds exhibit dark blue fluorescence, half-width is less than 60 nm, thenon-doped OLED device prepared by taking the material as a luminescent material produces dark blue emission, a starting voltage is 3.3 V, the maximum brightness is greater than 20,000 cd.m, the external quantum efficiency is still greater than 3% when the brightness is up to 10,000 cd.m, and the material is a dark blue light material with excellent performance.

Heterocyclic com pounds and organic light-emitting diode including the same

The present invention relates to a novel heterocyclic compound and an organic electroluminescent device comprising the same. The heterocyclic compound is represented by the following Chemical Formula 1, and the organic electroluminescent device including the heterocyclic compound has excellent driving voltage, luminous efficiency, and lifespan properties. Chemical Formula 1. (by machine translation)

Novel organic compounds for organic light-emitting diode and organic light-emitting diode including the same

The present invention relates to an organic light emitting compound represented by formula A and an organic light emitting diode including the same. Substituents A1 to A4, R1 to R17, X, Y, a, b, m, n, p, L1, and L2 are identical to as defined in the detailed description.