1026076-51-6

Basic information

• Product Name: 1,4-dimethyl 2-(methylamino)benzene-1,4-dicarboxylate
• Synonyms: 1,4-dimethyl 2-(methylamino)benzene-1,4-dicarboxylate
• CAS NO: 1026076-51-6
• Molecular Weight: 223.229
• Mol File: 1026076-51-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1,4-dimethyl 2-(methylamino)benzene-1,4-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-dimethyl 2-(methylamino)benzene-1,4-dicarboxylate(1026076-51-6)
• EPA Substance Registry System: 1,4-dimethyl 2-(methylamino)benzene-1,4-dicarboxylate(1026076-51-6)

Safety Data

• Hazardous Substances Data: 1026076-51-6(Hazardous Substances Data)

Upstream product

• 866995-99-5 (acetyl-methyl-amino)-terephthalic acid dimethyl ester 
• 5372-81-6 dimethyl aminoterephthalate 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 
• 5441-05-4 dimethyl acetamidoterephthalate 
• 10312-55-7 3-aminoterephthalic acid 
• 7647-01-0 hydrogenchloride 
• 1027493-73-7 (methyl-nitroso-amino)-terephthalic acid dimethyl ester 
• 7732-18-5 water 
• 1027081-40-8 2-(tert-Butoxycarbonyl-methyl-amino)-terephthalic acid dimethyl ester 
• 67-56-1 methanol 

Downstream Products

• 872264-96-5 methylamino-terephthalic acid-4-methyl ester 
• 1027493-73-7 (methyl-nitroso-amino)-terephthalic acid dimethyl ester 
• 52251-19-1 2-(N,N-dimethylamino)terephthlate dimethyl ester 

Relevant articles and documents

Systematic variation of the optical bandgap in titanium based isoreticular metal-organic frameworks for photocatalytic reduction of CO2 under blue light

A series of metal-organic frameworks isoreticular to MIL-125-NH2 were prepared, where the 2-amino-terephthalate organic links feature N-alkyl groups of increasing chain length (from methyl to heptyl) and varying connectivity (primary and secondary). The prepared materials display reduced optical bandgaps correlated with the inductive donor ability of the alkyl substituent as well as high photocatalytic activity towards the reduction of carbon dioxide under blue illumination operating over 120 h. Secondary N-alkyl substitution (isopropyl, cyclopentyl and cyclohexyl) exhibits larger apparent quantum yields than the primary N-alkyl analogs directly related to their longer lived excited-state lifetime. In particular, MIL-125-NHCyp (Cyp = cyclopentyl) exhibits a small bandgap (Eg = 2.30 eV), a long-lived excited-state (τ = 68.8 ns) and a larger apparent quantum yield (Φapp = 1.80%) compared to the parent MIL-125-NH2 (Eg = 2.56 eV, Φapp = 0.31%, τ = 12.8 ns), making it a promising candidate for the next generation of photocatalysts for solar fuel production based on earth-abundant elements.

PHOTO-REDOX TITANIUM CONTAINING ORGANIC FRAMEWORKS AND METHODS OF MAKING AND USE THEREOF

Disclosed herein are metal-organic frameworks and methods of making and use thereof.

1,3-dimethyl-7-substituted-quinazolinyl-2,4-diones, and synthesis method and application thereof

The invention discloses 1,3-dimethyl-7-substituted-quinazolinyl-2,4-diones. The structural general formula of the compounds is disclosed in the specification, wherein R1 is hydrogen or ethyl; and R2 is a benzene ring, benzene ring derivative, heterocyclic ring or aliphatic hydrocarbon. Part of compounds have favorable inhibiting activities for Candida albicans, Aspergillus flavus, Torula histolytica and Aspergillus fumigatus. The compounds have obvious inhibiting activities for chitin synthetase, have favorable antibacterial effects, and can be used for preparing drugs for anti-pathogenic microorganisms.