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1,1,1,3,3,3-hexafluoro-2-methoxy-2-(trifluoromethyl)propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66670-22-2

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66670-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66670-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,7 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66670-22:
(7*6)+(6*6)+(5*6)+(4*7)+(3*0)+(2*2)+(1*2)=142
142 % 10 = 2
So 66670-22-2 is a valid CAS Registry Number.

66670-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,3,3,3-hexafluoro-2-methoxy-2-(trifluoromethyl)propane

1.2 Other means of identification

Product number -
Other names Perfluor-tert.-butyl-methylether

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:66670-22-2 SDS

66670-22-2Upstream product

66670-22-2Downstream Products

66670-22-2Relevant academic research and scientific papers

Preparation and physicochemical properties of F-tert-butyl alkyl ethers

Takada, Naoto,Abe, Takashi,Sekiya, Akira

, p. 167 - 171 (2007/10/03)

As a part of studies on the development of CFCs alternatives, F-tert-butyl alkyl ethers [(CF3)3COMe and (CF3)3COEt] were prepared and their basic physicochemical properties were determined. They were prepared by alkylation of isolated (CF3)3CONa with dialkyl sulfates [(RO2)2SO2: R = CH3, C2H5] with good yields. It was found that the yields were affected by the kind of polyglymes used as a solvent. Tetraglyme was a much better solvent than diglyme for dissolving (CF3)3CONa, this fact being ascribed to the number of intramolecular oxygen atoms in polyglymes for coordination to Na+. A correlation between the structure of the F-butyl group of the ether, C4F9OR, and some physical properties was observed, in which an ether having an F-tert-butyl group has a lower boiling point and gaseous thermal conductivity compared with that having an F-n-butyl group.

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