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2378-08-7

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2378-08-7 Usage

General Description

Fluoropentachloroacetone is a synthetic chemical compound that is known for its strong irritant and toxic properties. It is a chlorinated derivative of acetone and contains five chlorine atoms and one fluorine atom. Due to its highly reactive nature, fluoropentachloroacetone has been extensively studied for its potential use as a chemical warfare agent. It is considered a severe skin and respiratory irritant and exposure to this compound can cause severe eye, skin, and respiratory irritation, as well as nausea, vomiting, and headache. Its potential use in chemical warfare and its harmful effects on human health highlight the importance of strict regulations and oversight on its production, use, and handling.

Check Digit Verification of cas no

The CAS Registry Mumber 2378-08-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,7 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2378-08:
(6*2)+(5*3)+(4*7)+(3*8)+(2*0)+(1*8)=87
87 % 10 = 7
So 2378-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C3Cl5FO/c4-2(5,6)1(10)3(7,8)9

2378-08-7SDS

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 1,1,1,3,3-pentachloro-3-fluoropropan-2-one

1.2 Other means of identification

Product number -
Other names FLUOROPENTACHLOROACETONE

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:2378-08-7 SDS

2378-08-7Relevant articles and documents

Synthesis of Halogenated Pyridines via the CuCl-Catalyzed Addition of Polyhaloacetonitriles to Olefins

Pews, R. Garth,Lysenko, Zenon

, p. 5115 - 5119 (2007/10/02)

Halogenated acetonitriles add smoothly to acrolein, methacrolein, and methacrolein dimethyl acetal in the presence of a catalytic amount of CuCl and triphenylphosphine, tri-n-butylphosphine, or triethylamine to give halogenated difunctional adducts.The adducts have been cyclized in high yields under acidic conditions to halogenated pyridines.

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