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64218-50-4

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64218-50-4 Usage

General Description

2-CHLORO-1-(4,5-DICHLORO-2-THIENYL)ETHAN-1-ONE is a chemical compound with the molecular formula C8H4Cl3O2S. It is a derivative of thienyl and is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 2-CHLORO-1-(4,5-DICHLORO-2-THIENYL)ETHAN-1-ONE is a chlorinated ketone that is primarily used as a building block for the production of various organic chemicals. However, it is important to handle this chemical with caution, as it can be harmful if ingested, inhaled, or comes into contact with skin or eyes. Proper safety measures should be taken when working with this compound to avoid any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 64218-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,1 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64218-50:
(7*6)+(6*4)+(5*2)+(4*1)+(3*8)+(2*5)+(1*0)=114
114 % 10 = 4
So 64218-50-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl3OS/c7-2-4(10)5-1-3(8)6(9)11-5/h1H,2H2

64218-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(4,5-dichlorothiophen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2,3-Dichlor-5-chloracetyl-thiophen

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:64218-50-4 SDS

64218-50-4Downstream Products

64218-50-4Relevant articles and documents

Bromothiophene Reactions. II. A Novel Rearrangement in the Zinc and Acetic Acid Reduction

Alvares-Insua, A. S.,Conde, S.,Corral, C.

, p. 713 - 716 (2007/10/02)

The elimination of the α-bromine atoms of the bromothienylethanolamine derivatives 2a, b, c, d with zinc and acetic acid unexpectedly involved a migration of the ethanolamine side chain from the 3 to the 2 position in the thiophene ring.Experiments carried out with simpler analogous compounds 3, 4 and 6 seem to indicate that this rearrangement takes place only in those cases in which the carbon atom of the side chain next to the ring supports an oxygen atom capable of being protonated in the reaction medium.A tentative mechanism is proposed to explain the experimental results.

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