Welcome to LookChem.com Sign In|Join Free
  • or
Phenol, 4,4'-(2,2,2-trifluoro-1-phenylethylidene)bis-, also known as 2,2,2-trifluoro-1-phenylethylidene-bisphenol or simply 4,4'-(2,2,2-trifluoro-1-phenylethylidene)bisphenol, is an organic compound with the chemical formula C20H14F3O2. It is a white crystalline solid that is soluble in organic solvents. Phenol, 4,4'-(2,2,2-trifluoro-1-phenylethylidene)bis- is primarily used as a monomer in the production of polycarbonates, which are high-performance plastics known for their strength, transparency, and durability. These polycarbonates find applications in various industries, including automotive, electronics, and construction, for the manufacturing of components such as lenses, CDs, DVDs, and protective casings. The compound is also valued for its thermal stability and resistance to chemicals, which contribute to the performance of the resulting polymers.

1882-01-5

Post Buying Request

1882-01-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1882-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1882-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1882-01:
(6*1)+(5*8)+(4*8)+(3*2)+(2*0)+(1*1)=85
85 % 10 = 5
So 1882-01-5 is a valid CAS Registry Number.

1882-01-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2,2,2-trifluoro-1-(4-hydroxyphenyl)-1-phenylethyl]phenol

1.2 Other means of identification

Product number -
Other names 1,1,1-Trifluor-2,2-bis-<4-hydroxy-phenyl>-2-phenyl-aethan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1882-01-5 SDS

1882-01-5Downstream Products

1882-01-5Relevant academic research and scientific papers

Fluorinated poly(arylene ether ketone)s for high temperature dielectrics

Shaver, Andrew T.,Yin, Kezhen,Borjigin, Hailun,Zhang, Wenrui,Choudhury, Shreya Roy,Baer, Eric,Mecham, Sue J.,Riffle,McGrath, James E.

, p. 199 - 204 (2016)

There is a need for polymeric capacitors with improved energy storage density and thermal stability. In this work, the effect of polymer molecular structure and symmetry on Tg, breakdown strength, and relative permittivity were investigated. A

One-Pot Trifluoromethylative Functionalization of Amides: Synthesis of Trifluoromethylated Bis(indolyl)arylmethanes and Triarylmethanes

Pandey, Vinay Kumar,Anbarasan, Pazhamalai

, p. 12328 - 12336 (2017/12/08)

Efficient and general one-pot trifluoromethylative functionalization of amides has been accomplished for the synthesis of various trifluoromethylated bis(indolyl)arylmethane, utilizing trifluoromethyltrimethylsilane and substituted indoles as nucleophiles. The developed reaction involves the in situ generation and trapping of a trifluoromethylated iminium ion, derived from the trifluoromethylated hemiaminal of amide, with various substituted indoles. This method has been successfully extended to the synthesis of diverse trifluoromethylated triarylmethanes employing phenols as nucleophiles. Furthermore, the potential of the method was demonstrated via the two-step synthesis of a trifluoromethylated analog of a hypolipidemic and anti-obesity agent.

1,1,1-Triaryl-2,2,2-trifluoroethanes and process for their synthesis

-

, (2008/06/13)

New 1,1,1-triaryl-2,2,2-trifluoroethanes in which the aryl radicals carry one or more substitutents have been prepared by condensation of trifluoroacetophenones with substituted phenyl compounds in the presence of catalytic quantities of trifluoromethylsu

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1882-01-5