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357-98-2

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357-98-2 Usage

General Description

1,1,2,3,3,3-Hexafluoropropoxybenzene is a chemical compound with the molecular formula C9H3F6O. It is a colorless liquid with a faint odor and is insoluble in water. 1,1,2,3,3,3-HEXAFLUOROPROPOXYBENZENE is primarily used as an intermediate in the manufacturing of other chemicals, particularly in the production of pharmaceuticals, agrochemicals, and industrial chemicals. It is also used as a solvent and as a reagent in organic synthesis. 1,1,2,3,3,3-Hexafluoropropoxybenzene is considered to have low toxicity, but it should be handled with caution and proper safety measures must be taken to prevent exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 357-98-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 357-98:
(5*3)+(4*5)+(3*7)+(2*9)+(1*8)=82
82 % 10 = 2
So 357-98-2 is a valid CAS Registry Number.

357-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,3,3,3-Hexafluoropropoxybenzene

1.2 Other means of identification

Product number -
Other names 1,1,2,3,3,3-HEXAFLUOROPROPOXYBENZENE

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:357-98-2 SDS

357-98-2Downstream Products

357-98-2Relevant articles and documents

Palladium(0)-catalyzed hydroalkoxylation of hexafluoropropene: Synthesis of hydrofluoroethers under neutral conditions

Matsukawa, Yasuhisa,Mizukado, Junji,Quan, Heng-Dao,Tamara, Masanori,Sekiya, Akira

, p. 1128 - 1130 (2005)

No vinyl ether by-products are formed in the palladium(0)-complex catalyzed hydroalkoxylation of hexafluoropropene (see scheme). Saturated hydrofluoro-ethers are selectively synthesized with alcohols or phenols under neutral conditions in the presence of

SPONTANEOUS REACTIONS OF POTASSIUM PHENOXIDE WITH DIBROMOPERFLUOROALKANES. FIRST EVIDENCE FOR BROMOPHILIC ATTACK ON C-Br BONDS BY THE PHENOXIDE ION.

Xingya, Li,Heqi, Pan,Xikui, Jiang

, p. 4937 - 4940 (2007/10/02)

In contrast to earlier reports, It has been found that dibromoperfluoroalkanes actually can react spontaneously with PhOK, yielding fluoroalkyl phenyl ethers as products.Evidence for an anionic chain mechanism involving a bromophilic attack by the phenoxyde ion is presented.

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