138377-34-1

Basic information

• Product Name: 2-CHLORO-3-HYDROXYBENZOTRIFLUORIDE
• Synonyms: 2-CHLORO-3-(TRIFLUOROMETHYL)PHENOL;2-CHLORO-3-HYDROXYBENZOTRIFLUORIDE;2-Chloro-3-hydroxybenzotrifluoride 98%;2-Chloro-3-hydroxybenzotrifluoride98%
• CAS NO: 138377-34-1
• Molecular Formula: C₇H₄ClF₃O
• Molecular Weight: 196.55
• EINECS: -0
• Product Categories: Phenol&Thiophenol&Mercaptan;Organic Building Blocks;Oxygen Compounds;Phenols;Building Blocks;C6 to C8;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
• Mol File: 138377-34-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 160 °C(lit.)
• Flash Point: 175 °F
• Appearance: /
• Density: 1.479 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.152mmHg at 25°C
• Refractive Index: n20/D 1.482(lit.)
• BRN: 9045773
• CAS DataBase Reference: 2-CHLORO-3-HYDROXYBENZOTRIFLUORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-3-HYDROXYBENZOTRIFLUORIDE(138377-34-1)
• EPA Substance Registry System: 2-CHLORO-3-HYDROXYBENZOTRIFLUORIDE(138377-34-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• RIDADR: 2810
• WGK Germany: 3
• HazardClass: IRRITANT
• PackingGroup: III
• Hazardous Substances Data: 138377-34-1(Hazardous Substances Data)

Usage

General Description

2-Chloro-3-(trifluoromethyl)phenol is an oxygen containing building block used in chemical synthesis.

InChI:InChI=1/C7H4ClF3O/c8-6-4(7(9,10)11)2-1-3-5(6)12/h1-3,12H

Downstream Products

• 280753-11-9 3-chloro-4-hydroxy-2-(trifluoromethyl)benzaldehyde 
• 846031-36-5 1-[2-chloro-3-(trifluoromethyl)phenyl]piperazine 
• 1466528-37-9 (R)-tert-butyl 1-(2-chloro-3-(trifluoromethyl)phenoxy)propan-2-ylcarbamate 
• 1466526-25-9 (R)-5-amino-N-(1-(2-chloro-3-(trifluoromethyl)phenoxy)propan-2-yl)-2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxamide 
• 1466528-38-0 (R)-1-(2-chloro-3-(trifluoromethyl)phenoxy)propan-2-amine hydrochloride 
• 954232-58-7 C₁₅H₁₇ClF₃NO₃ 

Relevant articles and documents

Process for the preparation of phenates substituted by halogen groups or of the corresponding phenols

This invention relates to a process for preparing phenates substituted by halogen groups of the corresponding phenols which comprises reacting a halo-substituted benzene with a powdered base having a particle size of less than 4 mm in the presence of an aprotic polar solvent.