198821-77-1

Basic information

• Product Name: (2-METHOXY-4-NITROPHENYL)METHANEDIOL DIACETATE
• Synonyms: (2-METHOXY-4-NITROPHENYL)METHANEDIOL DIACETATE;(ACETYLOXY)(2-METHOXY-4-NITROPHENYL)METHYL ACETATE;(2-Methoxy-4-nitrophenyl)Methylenediacetate
• CAS NO: 198821-77-1
• Molecular Formula: C₁₂H₁₃NO₇
• Molecular Weight: 283.23
• Mol File: 198821-77-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2-METHOXY-4-NITROPHENYL)METHANEDIOL DIACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: (2-METHOXY-4-NITROPHENYL)METHANEDIOL DIACETATE(198821-77-1)
• EPA Substance Registry System: (2-METHOXY-4-NITROPHENYL)METHANEDIOL DIACETATE(198821-77-1)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 198821-77-1(Hazardous Substances Data)

Usage

General Description

(2-METHOXY-4-NITROPHENYL)METHANEDIOL DIACETATE is a chemical compound with the molecular formula C11H13NO7. It is a diacetate ester of (2-methoxy-4-nitrophenyl)methanediol, which is a derivative of 4-nitrocatechol. (2-METHOXY-4-NITROPHENYL)METHANEDIOL DIACETATE is commonly used as a precursor in the synthesis of pharmaceutical compounds and in organic chemistry research. It is a white to off-white crystalline powder with a melting point of 128-130°C and is soluble in organic solvents. The compound has various potential applications in the pharmaceutical, chemical, and research industries due to its unique chemical properties and reactivity.

Upstream product

• 13120-77-9 2-methyl-5-nitroanisole 
• 64-19-7 acetic acid 
• 108-24-7 acetic anhydride 

Downstream Products

• 267405-89-0 3-[[3-Methoxy-4-(5-oxazolyl)phenyl]amino]-3-oxopropanoic Acid Ethyl Ester 
• 267405-38-9 [[3-Methoxy-4-(5-oxazolyl)phenyl]amino]oxoacetic Acid Ethyl Ester 
• 267406-37-1 3-[[3-Methoxy-4-(5-oxazolyl)phenyl]amino]-3-oxopropanoic acid 
• 267406-36-0 2-(3-methoxy-4-(oxazol-5-yl)phenylamino)-2-oxoacetic acid 

Relevant articles and documents

Substitution Effect on 2-(Oxazolinyl)-phenols and 1,2,5-Chalcogenadiazole -Annulated Derivatives: Emission-Color-Tunable, Minimalistic Excited-State Intramolecular Proton Transfer (ESIPT)-Based Luminophores

Minimalistic 2-(oxazolinyl)-phenols substituted with different electron-donating and -withdrawing groups as well as 1,2,5-chalcogenadiazole-annulated derivatives thereof were synthesized and investigated in regard to their emission behavior in solution as well as in the solid state. Depending on the nature of the incorporated substituent and its position, emission efficiencies were increased or diminished, resulting in AIE or ACQ characteristics. Single-crystal analysis revealed J- and H-type packing motifs and a so-far undescribed isolation of ESIPT-based fluorophores in the keto form.

Novel diamide-based inhibitors of IMPDH

A series of novel amide-based small molecule inhibitors of inosine monophosphate dehydrogenase is described. The synthesis and the structure-activity relationships (SARs) derived from in vitro studies are presented.