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Benzene, 1,4-bis(trifluoromethoxy)-, also known as 1,4-bis(trifluoromethoxy)benzene or BTFB, is an organic compound with the chemical formula C8H6F6O2. It is a colorless liquid at room temperature and is derived from benzene by substituting two hydrogen atoms with trifluoromethoxy groups. BTFB is a versatile intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is known for its unique properties, such as its high boiling point, low toxicity, and excellent solubility in organic solvents. Due to its stability and reactivity, BTFB is widely used in the production of various fluorinated compounds, making it an important building block in the field of fluorochemistry.

660-36-6

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660-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 660-36-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 660-36:
(5*6)+(4*6)+(3*0)+(2*3)+(1*6)=66
66 % 10 = 6
So 660-36-6 is a valid CAS Registry Number.

660-36-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Bis(trifluoromethoxy)benzene

1.2 Other means of identification

Product number -
Other names Hexa-Si-aethyl-Si,Si'-butadiindiyl-bis-silan

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:660-36-6 SDS

660-36-6Downstream Products

660-36-6Relevant academic research and scientific papers

TRIFLUORMETHYLIERUNGSREAKTIONEN VON CF3I, Te(CF3)2, Sb(CF3)3, Hg(CF3)2, UND Cd(CF3)2*D MIT FURAN, THIOPHEN, PYRROL UND p-BENZOCHINON

Naumann, Dieter,Kischkewitz, Juergen

, p. 265 - 281 (2007/10/02)

The trifluoromethylation reactions of Cd(CF3)2*glyme, Hg(CF3)2, Sb(CF3)3, CF3I, and Te(CF3)2 with furan, thiophene, pyrrol, and p-benzoquinone are compared under similar conditions.During the photochemical reactions the reactivity increases in the series

Preparation of aryl trifluoromethyl ethers

-

, (2008/06/13)

A one-step process for the synthesis of aryl trifluoromethyl ethers by reacting phenol or certain substituted phenols with a perhalomethane and hydrogen fluoride is provided. The compounds produced by the process of this invention are useful intermediates in the production of dyestuffs and pharmaceuticals.

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