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1,3-Oxathiolane-2-acetamide, 2-methyl-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67980-06-7

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67980-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67980-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,8 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67980-06:
(7*6)+(6*7)+(5*9)+(4*8)+(3*0)+(2*0)+(1*6)=167
167 % 10 = 7
So 67980-06-7 is a valid CAS Registry Number.

67980-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methyl-1,3-oxathiolan-2-yl)-N-phenylacetamide

1.2 Other means of identification

Product number -
Other names 2-methyl-N-phenyl-1,3-oxathiolane-2-acetamide

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:67980-06-7 SDS

67980-06-7Relevant academic research and scientific papers

Formation of a Thiirane and a 1,3-Oxathiolane S-Oxide from Thermolysis of a Thiosulfinic S-Ester

Hahn, Hoh-Gyu,Lee, Wha Suk

, p. 630 - 645 (2007/10/02)

Oxidation of 1.3-oxathiolane 1 with aqueous hydrogen peroxide in the presence of benzeneseleninic acid gave the cis sulfoxide 2 in high yield.The sulfenic acid 6 and thioaldehyde 5 generated by thermolysis of the thiosulfinic S-ester 4 underwent intramole

New synthesis of carboxin and oxycarboxin pesticides: application to the preparation of their new analogues substituted at the C-2 methyl group

Caputo, Romualdo,Ferreri, Carla,Guaragna, Annalisa,Palumbo, Giovanni,Pedatella, Silvana

, p. 1971 - 1974 (2007/10/02)

A new synthesis of carboxin 1a and its 4,4-dioxide derivative, oxycarboxin 2a, has been devised via N-bromosuccinimide-promoted oxidative rearrangement of acetoacetanilide 1,3-oxathiolane 3.The replacement of N-bromosuccinimide with molecular bromine leads to the formation, from compound 3, of a C-2 bromomethylcarboxin derivative 1b.The latter is conveniently exploited to prepare a new class of carboxins and oxycarboxins (after oxidation of the sulfur) substituted at the C-2 methyl, by replacement of the bromine atom with various nucleophiles.

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