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3-Methoxythiobenzoic acid S-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28145-59-7

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28145-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28145-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,4 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28145-59:
(7*2)+(6*8)+(5*1)+(4*4)+(3*5)+(2*5)+(1*9)=117
117 % 10 = 7
So 28145-59-7 is a valid CAS Registry Number.

28145-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-methoxythiobenzoate

1.2 Other means of identification

Product number -
Other names m-Methoxythiobenzoesaeure-S-aethylester

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:28145-59-7 SDS

28145-59-7Upstream product

28145-59-7Downstream Products

28145-59-7Relevant academic research and scientific papers

Process for the preparation of 1,2-dioxetane compounds and novel sulfur-substituted 1,2-dioxetane compounds as intermediates

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, (2008/06/13)

A process for producing a stable triggerable dioxetane comprising; (a) reacting a vinyl sulfide compound containing a sulfur-substituent SR4, wherein R4 is an organic group containing 1 to 20 carbon atoms and optionally heteroato

Vinyl sulfide compounds and a process for their preparation

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, (2008/06/13)

Vinyl sulfides bearing protected arlyoxy substituents and a process for their preparation are provided. In the process a vinyl sulfide is formed by coupling a ketone compound and a thioester compound with a low valent titanium reagent to form both carbon-

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