73733-02-5

Basic information

• Product Name: 2-isopropoxynaphthalen-1-ol
• Synonyms: 2-isopropoxynaphthalen-1-ol
• CAS NO: 73733-02-5
• Molecular Weight: 202.253
• Mol File: 73733-02-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-isopropoxynaphthalen-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-isopropoxynaphthalen-1-ol(73733-02-5)
• EPA Substance Registry System: 2-isopropoxynaphthalen-1-ol(73733-02-5)

Safety Data

• Hazardous Substances Data: 73733-02-5(Hazardous Substances Data)

Upstream product

• 879-15-2 2-diazo-1,2-naphthoquinone 
• 67-63-0 isopropyl alcohol 

Relevant articles and documents

TRANSFORMATIONS OF o-NAPHTHOQUINONE DIAZIDES IN ALIPHATIC ALCOHOLS

During photodecomposition and thermal decomposition in hydroxyl-containing media (alcohols, water) o-naphthoquinone diazides in electronically excited and vibrationally excited states eliminate nitrogen, forming the corresponding ketocarbenes.The singlet ketocarbenes undergo intramolecular transformation (with ring contraction and the formation of 3-indenecarboxylic acid or its esters) and intermolecular transformation, forming 1,2-hydroxyalkoxynaphthalenes in reaction with alcohols.The triplet ketocarbenes undergo intermolecular transformations, forming 1- or 2-hydroxynaphthalenes.The composition and ratio of the final products from the decomposition of o-naphthoquinone diazides in alcohols depend significantly on the nature of the alcohol, the presence of oxygen, the presence of radical acceptors, and the spectral composition of the exciting light.