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1,3-Dioxolane, 2-(2-chloroethyl)-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57398-28-4

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57398-28-4 Usage

Physical state

Clear, colorless liquid

Odor

Faint

Usage

Commonly used as a solvent in various industrial processes

Classification

Alkylating agent

Function

Ability to transfer alkyl groups from one molecule to another

Potential hazard

Mutagen

Health effects

Demonstrated carcinogenic effects in animal studies

Safety

Hazardous substance that should be handled with caution and in accordance with appropriate safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 57398-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,9 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57398-28:
(7*5)+(6*7)+(5*3)+(4*9)+(3*8)+(2*2)+(1*8)=164
164 % 10 = 4
So 57398-28-4 is a valid CAS Registry Number.

57398-28-4SDS

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-(2-chloroethyl)-2-methyl-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 1-chloro-3,3-ethylenedioxybutane

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:57398-28-4 SDS

57398-28-4Downstream Products

57398-28-4Relevant academic research and scientific papers

A Synthetic Approach to (+/-)-Tridentoquinone

Brown, Roger F. C.,Robinson, Andrea J.

, p. 515 - 530 (1995)

Synthesis of the ansa-bridged benzofuranquinone (+/-)-tridentoquinone (+/-)-(1) is approached by constriction of a C4 methyl ketone chain at the 3-position of 6-bromo-4,5,7-trimethoxy-2,2-dimethyl-2,3-dihydrobenzofuran (10) and alkylation at its 6-position leading after modification to a dimethyl C10 aldehydic chain.Closure of the ansa bridge by McMurry coupling of the aldehyde and ketone groups of the intermediate (33) with C8K/TiCl3 appears to occur, but in poor yield and with uncertain stereochemistry, and the synthesis has not been completed.

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