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Cycloheptane, tetradecafluoro-, also known as perfluorocycloheptane, is a halogenated hydrocarbon with the chemical formula C7F14. It is a colorless, odorless, and non-toxic liquid at room temperature. Cycloheptane, tetradecafluoro- is characterized by the presence of seven fluorine atoms attached to each carbon atom in a cycloheptane ring structure. Due to its unique properties, such as high chemical stability, low reactivity, and excellent thermal and oxidative stability, perfluorocycloheptane finds applications in various industries, including electronics, aerospace, and chemical processing. It is also used as a refrigerant, heat transfer medium, and dielectric fluid. However, it is essential to handle Cycloheptane, tetradecafluoro- with care, as it can contribute to environmental concerns like global warming and ozone depletion due to its high global warming potential.

355-59-9

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355-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 355-59-9 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 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 355-59:
(5*3)+(4*5)+(3*5)+(2*5)+(1*9)=69
69 % 10 = 9
So 355-59-9 is a valid CAS Registry Number.

355-59-9SDS

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 1,1,2,2,3,3,4,4,5,5,6,6,7,7-tetradecafluorocycloheptane

1.2 Other means of identification

Product number -
Other names tetradecafluoro-cycloheptane

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:355-59-9 SDS

355-59-9Downstream Products

355-59-9Relevant academic research and scientific papers

POLYFLUORO-COMPOUNDS BASED ON THE CYCLOHEPTANE RING SYSTEM. PART 1. COMPOUNDS DERIVED FROM TRIDECAFLUOROCYCLOHEPTANE

Oliver, John A.,Stephens, Robert,Tatlow, John Colin

, p. 21 - 30 (2007/10/02)

Partial fluorination of cycloheptane by cobaltic fluoride gave a mixture of polyfluorides, of which tridecafluorocycloheptane was present in significant proportions.With aqueous alkali this afforded dodecafluorocycloheptene, which with lithium aluminium hydride gave 1H-undecafluorocyclohept-1-ene.Each of these cyclo-olefins was oxidised to decafluoropimelic acid.Methanol/KOH reacted with dodecafluorocycloheptene to give mainly 1-methoxy-undecafluorocyclohept-1-ene together with ca 15percent of the 3-methoxy-isomer, and some 1,2-dimethoxydecafluorocyclohept-1-ene.The 1-methoxy-1-ene and cobaltic fluoride gave 1-methoxy- and 1-fluoromethoxytridecafluorocycloheptanone: the former was demethylated by sulphuric acid to dodecafluorocycloheptanone.The dichloro-adduct of the perfluoro-olefin was reduced by lithium aluminium hydride to a complex mixture, from which 1H/2H- and 1H,2H-dodecafluorocycloheptane were isolated.

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