153034-28-7

Basic information

• Product Name: 3,5-di-tert-butyl-2-[(prop-2-yn-1-yl)oxy]benzaldehyde
• Synonyms: 3,5-di-tert-butyl-2-[(prop-2-yn-1-yl)oxy]benzaldehyde
• CAS NO: 153034-28-7
• Molecular Weight: 272.387
• Mol File: 153034-28-7.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: 3,5-di-tert-butyl-2-[(prop-2-yn-1-yl)oxy]benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-di-tert-butyl-2-[(prop-2-yn-1-yl)oxy]benzaldehyde(153034-28-7)
• EPA Substance Registry System: 3,5-di-tert-butyl-2-[(prop-2-yn-1-yl)oxy]benzaldehyde(153034-28-7)

Safety Data

• Hazardous Substances Data: 153034-28-7(Hazardous Substances Data)

Upstream product

• 37942-07-7 3,5-di-tert-butyl-2-hydroxybenzaldehyde 
• 106-96-7 propargyl bromide 

Downstream Products

• 153034-29-8 2-propargyloxy-3,5-di-t-butylbenzyl alcohol 
• 1383545-94-5 dimethyl 6,8-di-tert-butyl-3-phenyl-1,9b-dihydrocyclopenta[c]chromene-2,2(4H)-dicarboxylate 
• 1383545-76-3 dimethyl 2-(3,5-di-tert-butyl-2-((3-phenylprop-2-yn-1-yl)oxy)phenyl)cyclopropane-1,1-dicarboxylate 
• 1334473-08-3 5,7-di-tert-butyl-2-(2-(4-chlorophenyl)-2-oxoethyl)-2-methylbenzofuran-3(2H)-one 
• 1279702-88-3 C₂₅H₃₈O₅ 
• 1279702-74-7 C₂₂H₃₄O₃ 
• 1224712-94-0 6,8-di-tert-butyl-3-[2-(4-chloro-phenyl)-2-oxo-ethyl]-chroman-4-one 
• 153034-41-4 2-propargyloxy-3,5-di-t-butylbenzyl azide 
• 153034-39-0 2-propargyloxy-3,5-di-t-butylbenzyl chloride 
• 1415717-51-9 2-(3,5-di-tert-butyl-2-(prop-2-ynyloxy)phenyl)furan 

Relevant articles and documents

Synthesis and spectral study of a new family of 2,5-diaryltriazoles having restricted rotation of the 5-aryl substituent

Efficient synthesis of 2,5-diaryl substituted 4-azido-1,2,3-triazoles by the reaction of sodium azide with dichlorosubstituted diazadienes was demonstrated. The optical properties of the prepared azidotriazoles were studied to reveal a luminescence maximu

“On water” cascade synthesis of benzopyranopyrazoles and their macrocycles

Reported herein is an intramolecular 1,3-dipolar cycloaddition strategy for rapid entry into benzopyranopyrazoles (BPP) on water medium as “open flask chemistry” approach. The in situ generation of diazo functionality in two-step sequence from the appropr

A facile one-pot regioselective synthesis of functionalized novel benzo[f]chromeno[4,3-b][1,7]naphthyridines and benzo[f][1,7]naphthyridines via an imino Diels-Alder reaction

A novel series of functionalized 13H-benzo[f]chromeno[4,3-b][1,7]naphthyridines and 1,3-diphenylbenzo[f][1,7]naphthyridines have been synthesized by an efficient regioselective one-pot multicomponent synthesis through intra and intermolecular imino Diels-