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554-21-2

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554-21-2 Usage

Common uses

Reagent in organic synthesis
Solvent in various industrial processes

Chemical properties

Highly reactive
Strong oxidizing properties

Applications

Precursor for the synthesis of other chemicals
Used in the production of pharmaceuticals and pesticides

Hazards

Toxic compound
Can cause skin and respiratory irritation
Potential environmental hazards if improperly disposed of

Safety measures

Handle with caution
Follow proper safety protocols and measures when working with this chemical
Please note that the information provided is based on the material given and may not be exhaustive. It is always recommended to consult a reliable source or a professional chemist for more detailed information on the properties and handling of specific chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 554-21-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 554-21:
(5*5)+(4*5)+(3*4)+(2*2)+(1*1)=62
62 % 10 = 2
So 554-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H2Cl6O3/c6-4(7,8)1-2(12)14-3(13-1)5(9,10)11/h1,3H

554-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Dioxolan-4-one, 2,5-bis-trichloromethyl-

1.2 Other means of identification

Product number -
Other names 2,5-Bis-pentafluoraethyl-1,3,4-oxadiazol

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:554-21-2 SDS

554-21-2Relevant articles and documents

Carbonylation of trichloroacetaldehyde (chloral) in concentrated sulfuric acid: Stereocontrolled synthesis of cis- and trans-2,5-bis(trichloromethyl)-1,3-dioxolan-4-one

Mori, Sadayuki,Emura, Kazuhiro,Kano, Motoaki,Kudo, Kiyoshi,Komatsu, Koichi,Sugita, Nobuyuki

, p. 8977 - 8982 (2007/10/02)

Carbonylation of trichloroacetaldehyde(chiral) in concentrated sulfuric acid readily gave 2,5-bis(trichloromethyl-1,3-dioxolan-4-ones (cis and trans) and 3,3,3-trichloro-2-hydroxypropanoic acid. The cis isomer was isolated for the first time, and confirmed by X-ray structural analysis. The cis/trans ratio of dioxolanones largely depended upon the concentration of sulfuric acid. Highly diastereoselective formation of the dioxolanones was achieved with 99wt% sulfuric acid (cis:trans = 95:5) or with 90wt% sulfuric acid (0:100).

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