40053-98-3

Basic information

• Product Name: o-Hydroxybenzylchloride
• Synonyms: o-Hydroxybenzylchloride
• CAS NO: 40053-98-3
• Molecular Formula: C₇H₇ClO
• Molecular Weight: 142.5829
• Mol File: 40053-98-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 240.7 °C at 760 mmHg
• Flash Point: 99.3 °C
• Appearance: /
• Density: 1.233 g/cm³
• PKA: 9.46±0.35(Predicted)
• CAS DataBase Reference: o-Hydroxybenzylchloride(CAS DataBase Reference)
• NIST Chemistry Reference: o-Hydroxybenzylchloride(40053-98-3)
• EPA Substance Registry System: o-Hydroxybenzylchloride(40053-98-3)

Safety Data

• Hazardous Substances Data: 40053-98-3(Hazardous Substances Data)

Usage

General Description

o-Hydroxybenzylchloride is a chemical compound with the molecular formula C7H7ClO. It is a benzyl chloride derivative with a hydroxyl group attached to the ortho position of the benzene ring. o-Hydroxybenzylchloride is commonly used in organic synthesis as a building block for the preparation of pharmaceuticals, agrochemicals, and dyes. It is also utilized in the production of polymers and other industrial chemicals. o-Hydroxybenzylchloride is a versatile intermediate that finds application in various chemical processes and reactions.

Upstream product

• 90-01-7 salicylic alcohol 

Downstream Products

• 50375-72-9 diethyl 2-hydroxybenzylphosphonate 
• 14714-50-2 2-hydroxybenzyl cyanide 
• 90-02-8 salicylaldehyde 

Relevant articles and documents

Novel 1,3,5-triazinyl aminobenzenesulfonamides incorporating aminoalcohol, aminochalcone and aminostilbene structural motifs as potent anti-vre agents, and carbonic anhydrases i, ii, vii, ix, and xii inhibitors

A series of 1,3,5-triazinyl aminobenzenesulfonamides substituted by aminoalcohol, ami-nostilbene, and aminochalcone structural motifs was synthesized as potential human carbonic an-hydrase (hCA) inhibitors. The compounds were evaluated on their inhibition

Immonium salts and derivatives thereof

There are provided: novel aryloxy immonium salts, prepared by the reaction of their corresponding haloformates with amides; and phenolic compositions corresponding to the aryloxy immonium salts. These novel aryloxy immonium salts and their corresponding phenolic compositions have utility as chemical intermediates, antioxidants, stabilizers and antibacterials.