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1-Chloroperfluoroheptane, also known as C7F15Cl, is a colorless, volatile liquid with a molecular formula of C7ClF15. It is a member of the perfluoroalkane family, characterized by the presence of a carbon-chlorine bond and seven fluorine atoms attached to a carbon chain. This chemical is primarily used as a refrigerant, fire extinguishing agent, and in the production of other perfluorinated compounds. Due to its high chemical stability, low toxicity, and non-flammability, 1-chloroperfluoroheptane has found applications in various industrial processes. However, it is essential to handle 1-Chloroperfluoroheptane with care, as it can contribute to environmental concerns such as ozone depletion and global warming due to its long atmospheric lifetime and potential to release greenhouse gases.

375-89-3

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375-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 375-89-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 375-89:
(5*3)+(4*7)+(3*5)+(2*8)+(1*9)=83
83 % 10 = 3
So 375-89-3 is a valid CAS Registry Number.

375-89-3SDS

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 1-Chloroperfluoroheptane

1.2 Other means of identification

Product number -
Other names 1-Chlor-pentadecafluor-heptan

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:375-89-3 SDS

375-89-3Downstream Products

375-89-3Relevant academic research and scientific papers

HALOGEN FLUOROSULFATE REACTIONS WITH FLUOROCARBONS

Shack, Carl J.,Christe, K. O.

, p. 63 - 74 (2007/10/02)

The scope of the reaction of simple fluorocarbon halides with chlorine fluorosulfate and mixtures of chlorine and bromine fluorosulfate to produce RfOSO2F compounds has been investigated.It is shown that in many cases even primary chlorine in -CF2Cl groups can be replaced by -OSO2F.Primary bromine or iodine in -CF2X are more readily replaced.The mechanism of this replacement reaction has been established by the isolation of the metastable iodine III intermediate RfI(OSO2F)2.Neither secondary chlorine nor bromine in -CFX- groups is affected.With the secondary iodide, i-C3F7I, the salt + - is formed.Furthermore, it has been found that ClOSO2F is capable of converting fluorocarbon acids or their derivatives into fluorocarbon halides.A combination of these two ClOSO2F reactions with the known conversion of RfCF2OSO2F to the corresponding fluorocarbon acid offers a novel, high yield chain shortening reaction for the otherwise unreactive fluorocarbon halides according to:

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