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593-14-6

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593-14-6 Usage

General Description

1-Chloro-8-fluorooctane is a chemical compound with the molecular formula C8H16ClF. It is a type of organofluorine compound and belongs to the family of chloroalkanes. This chemical is used as a solvent in various industrial applications and as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is a colorless liquid with a faint, sweet odor and is insoluble in water but soluble in organic solvents. 1-Chloro-8-fluorooctane is flammable and can release toxic fumes when heated to decomposition. It is important to handle this chemical with care and in accordance with proper safety procedures.

Check Digit Verification of cas no

The CAS Registry Mumber 593-14-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 593-14:
(5*5)+(4*9)+(3*3)+(2*1)+(1*4)=76
76 % 10 = 6
So 593-14-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H16ClF/c9-7-5-3-1-2-4-6-8-10/h1-8H2

593-14-6SDS

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-chloro-8-fluorooctane

1.2 Other means of identification

Product number -
Other names 1-chloro-8-fluoro-octane

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:593-14-6 SDS

593-14-6Relevant articles and documents

Halogen Exchange Reaction of Aliphatic Fluorine Compounds with Organic Halides as Halogen Source

Mizukami, Yuki,Song, Zhiyi,Takahashi, Tamotsu

supporting information, p. 5942 - 5945 (2016/01/09)

The halogen exchange reaction of aliphatic fluorine compounds with organic halides as the halogen source was achieved. Treatment of alkyl fluorides (primary, secondary, or tertiary fluorides) with a catalytic amount of titanocene dihalides, trialkyl aluminum, and polyhalomethanes (chloro or bromo methanes) as the halogen source gave the corresponding alkyl halides in excellent yields under mild conditions. In the case of a fluorine/iodine exchange, no titanocene catalyst is needed. Only C-F bonds are selectively activated under these conditions, whereas alkyl chlorides, bromides, and iodides are tolerant to these reactions.

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