379-18-0

Basic information

• Product Name: ALPHA-(TRIFLUOROMETHYL)BENZHYDROL
• Synonyms: A-(TRIFLUOROMETHYL)BENZHYDROL;DIPHENYL(TRIFLUOROMETHYL)CARBINOL;2,2,2-TRIFLUORO-1,1-(DIPHENYL)ETHANOL;ALPHA-(TRIFLUOROMETHYL)BENZHYDROL;-(Trifluoromethyl)benzhydrol;NSC42678;α-(triflouromethyl)benzhydrol
• CAS NO: 379-18-0
• Molecular Formula: C₁₄H₁₁F₃O
• Molecular Weight: 252.23
• Mol File: 379-18-0.mol
• Article Data: 51

Chemical Properties

• Melting Point: 74°C
• Boiling Point: 327.8 °C at 760 mmHg
• Flash Point: 135.4 °C
• Appearance: /
• Density: 1.26 g/cm³
• Vapor Pressure: 7.97E-05mmHg at 25°C
• Refractive Index: 1.529
• PKA: 11.10±0.10(Predicted)
• CAS DataBase Reference: ALPHA-(TRIFLUOROMETHYL)BENZHYDROL(CAS DataBase Reference)
• NIST Chemistry Reference: ALPHA-(TRIFLUOROMETHYL)BENZHYDROL(379-18-0)
• EPA Substance Registry System: ALPHA-(TRIFLUOROMETHYL)BENZHYDROL(379-18-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 379-18-0(Hazardous Substances Data)

Usage

General Description

ALPHA-(TRIFLUOROMETHYL)BENZHYDROL is a chemical compound with the molecular formula C14H11F3O. It is a white solid with a molecular weight of 250.23 g/mol. ALPHA-(TRIFLUOROMETHYL)BENZHYDROL is commonly used in pharmaceutical and chemical research as a building block for the synthesis of various organic compounds. It also has potential applications in the development of agrochemicals and other industrial products. ALPHA-(TRIFLUOROMETHYL)BENZHYDROL is known for its unique properties and is the subject of ongoing research to explore its potential uses in various fields.

InChI:InChI=1/C14H11F3O/c15-14(16,17)13(18,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,18H

Upstream product

• 383-63-1 ethyl trifluoroacetate, 
• 431-47-0 trifluoroacetic acid-methyl ester 
• 591-51-5 phenyllithium 
• 434-45-7 2,2,2-Trifluoroacetophenone 
• 108-86-1 bromobenzene 
• 119-61-9 benzophenone 
• 75-46-7 trifluoromethan 
• 75-63-8 Bromotrifluoromethane 
• 96236-02-1 (trifluoromethyl)diphenylmethyl bromide 
• 118143-24-1 2,2,2-trifluoro-1,1-diphenyl-1-(trimethylsilyloxy)ethane 
• 1586-73-8 tris(trimethylsilyl)amine 
• 345959-36-6 1-(4-benzylpiperazin-1-yl)-2, 2, 2-trifluoroethanol 
• 2314-97-8 iodotrifluoromethane 
• 445476-82-4 N,N-dimethyl-(1-phenyl-2,2,2-trifluoroethoxytrimethylsilyl)-amine 

Downstream Products

• 384-94-1 1,1'-(2,2,2-trifluoro-1,1-ethanediyl)dibenzene 
• 7723-95-7 2,2,2-trifluoro-1,1-bis-(4-nitro-phenyl)-ethanol 
• 630-71-7 4,4'-dichloro-α-phenyl-α-(trifluoromethyl)benzenemethanol 
• 427-57-6 dimethyl-[2-(2,2,2-trifluoro-1,1-diphenyl-ethoxy)-ethyl]-amine 
• 427-62-3 diethyl-[3-(2,2,2-trifluoro-1,1-diphenyl-ethoxy)-propyl]-amine 
• 427-60-1 dibutyl-[2-(2,2,2-trifluoro-1,1-diphenyl-ethoxy)-ethyl]-amine 
• 96235-96-0 2,2,2-Trifluoro-1,1-diphenylethanol-4-methylbenzenesulfonate 
• 89196-84-9 α-(trifluoromethyl)diphenylmethyl cation 
• 96236-02-1 (trifluoromethyl)diphenylmethyl bromide 
• 1995-76-2 N-(2,2,2-trifluoro-1,1-diphenylethyl)acetamide 
• 112881-91-1 2,2,2-Trifluoro-1,1-diphenylethanethiol 
• 863911-76-6 {2-hydroxymethyl-3-[2-(2,2,2-trifluoro-1,1-diphenylethylsulfanyl)ethyl]benzofuran-7-yloxy}acetic acid methyl ester 
• 863911-72-2 {2-(tetrahydropyran-2-yloxymethyl)-3-[2-(2,2,2-trifluoro-1,1-diphenylethylsulfanyl)ethyl]benzofuran-7-yloxy}acetic acid methyl ester 
• 112882-09-4 2,2,2-Trifluoro-1,1-diphenyl-ethanesulfonic acid 2-benzyloxy-ethyl ester 

Relevant articles and documents

Chiral trifluoromethylphosphines: A new stereoselective synthesis of Josiphos-type ligands containing two stereogenic phosphorus atoms

Intramolecular nucleophilic substitution of a trifluoromethyl group to form a 1,2-diphosphole derivative followed by the sequential addition of an alkylating agent and a carbanion are the key steps in the stereoselective synthesis of novel ferrocenyl diph

NOVEL METHOD FOR PRODUCING PERFLUOROALKYLATING AGENTS USING MONOHYDROPERFLUOROALKANE AS STARTING MATERIAL, AND METHOD FOR PRODUCING AROMATIC PERFLUOROALKYL COMPOUND USING THE SAME

PROBLEM TO BE SOLVED: To provide a simple method for producing trifluoromethyltriol borate potassium from trifluoromethane. SOLUTION: There is provided a method for producing a compound represented by the formula [7], comprising: reacting a monohydroperfluoroalkane with a base and trialkyl borate in an organic solvent; and then reacting the reaction solution with triol. [In the formula, RF is an alkyl group such as a linear chain of C1-2, and a perfluoroalkyl group in which all H on C is substituted with F; R6 is H or a C1-2 linear alkyl group, or the like; M may be a metal or the like belonging to Group I, Group II, Group III, Group IV, Group V, Group VI, Group VII, Group VIII, Group IX, Group X, Group XI, Group XII, and Group XIII in the periodic table of elements, and they may be a single substance or a mixture of a plurality of substances and y corresponds to the oxidation number of the substance represented by M.] SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

NOVEL METHOD FOR PRODUCING PERFLUOROALKYLATING AGENTS USING MONOHYDROPERFLUOROALKANE AS STARTING MATERIAL, AND METHOD FOR PRODUCING AROMATIC PERFLUOROALKYL COMPOUNDS USING THE SAME

To provide a simple method for producing silylated trifluoromethylcarbinol from trifluoromethane.SOLUTION: There is provided a method for producing a compound represented by the formula [1], in which the compound is obtained by reacting a monohydroperfluoroalkane, a carbonyl compound, and NaH in an organic solvent and then reacting the reaction solution with a silylating agent. [In the formula, RF is an alkyl group such as a linear chain of C1 to 2, and a perfluoroalkyl group in which all H on C is substituted with F; R1 and R2 are independently alkyl groups such as a linear chain of H or C1 to 2, or the like respectively; R1 and R2 may be integrated to form a ring; and R3, R4 and R5 are independently H or C1 to 2 linear alkyl groups, or the like respectively.]SELECTED DRAWING: None