5342-97-2

Basic information

• Product Name: tert-Butyl 3,5-dinitrobenzoate
• Synonyms: TERT-BUTYL 3,5-DINITROBENZOATE;3,5-DINITRO-BENZOIC ACID TERT-BUTYL ESTER
• CAS NO: 5342-97-2
• Molecular Formula: C₁₁H₁₂N₂O₆
• Molecular Weight: 268.22
• Mol File: 5342-97-2.mol
• Article Data: 9

Chemical Properties

• Melting Point: 142.5-143.5 °C
• Boiling Point: 376.5 °C at 760 mmHg
• Flash Point: 161.3 °C
• Appearance: /
• Density: 1.337 g/cm³
• Vapor Pressure: 7.22E-06mmHg at 25°C
• Refractive Index: 1.561
• CAS DataBase Reference: tert-Butyl 3,5-dinitrobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-Butyl 3,5-dinitrobenzoate(5342-97-2)
• EPA Substance Registry System: tert-Butyl 3,5-dinitrobenzoate(5342-97-2)

Safety Data

• Hazardous Substances Data: 5342-97-2(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 4415, 1994 DOI: 10.1016/S0040-4039(00)73371-5

InChI:InChI=1/C11H12N2O6/c1-11(2,3)19-10(14)7-4-8(12(15)16)6-9(5-7)13(17)18/h4-6H,1-3H3

Upstream product

• 99-34-3 3,5-dinitrobenzoic acid 
• 115-11-7 isobutene 
• 19756-72-0 tert-butyl 4-nitrobenzoate 
• 82251-69-2 3,5-dinitrobenzoic benzenesulphonic mixed anhydride 
• 6226-55-7 sodium 3,5-dinitrobenzoate 
• 75-65-0 tert-butyl alcohol 
• 865-47-4 potassium tert-butylate 
• 99-33-2 3,5-dinitrobenoyl chloride 
• 409322-21-0 3,5-dinitro-benzoic acid-(isobutyl-nitroso-amide) 

Downstream Products

• 99-34-3 3,5-dinitrobenzoic acid 
• 115-11-7 isobutene 
• 170030-61-2 tert-butyl 3,5-diaminobenzoate 
• 1400575-65-6 C₄₉H₆₈N₆O₁₀ 
• 1400575-66-7 C₄₅H₆₀N₆O₁₀ 
• 1400575-67-8 C₄₈H₆₂N₆O₁₀ 

Relevant articles and documents

Innovative Multipodal Ligands Derived from Tr?ger's Bases for the Sensitization of Lanthanide(III) Luminescence

Herein, the synthesis and characterization of the first family of multipodal ligands with a Tr?ger's base framework designed for the preparation of luminescent lanthanide(III) complexes are reported. Eight ligands were designed and synthesized using diffe

A novel, general route to the synthesis of carboxylic acid esters and thiolesters

Carboxylic acids were conveniently esterified with alcohols and thiols by the use of triphenylphosphine and N-bromo/Iodo succinimide to afford the corresponding esters and thiol esters.

REAGENTS AND SYNTHETIC METHODS 28. MODIFIED PROCEDURES FOR ANHYDRIZATION, ESTERIFICATION AND THIOLESTERIFICATION OF CARBOXYLIC ACIDS BY MEANS OF AVAILABLE PHOSPHORUS REAGENTS.

Carboxylic acid anhydrides, esters and thiol esters are obtained by a one-pot method from carboxylic acids and alcohols or thiol by means of phosphorus oxychloride or phenyl dichlorophosphoridate reagents.