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201017-90-5

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201017-90-5 Usage

General Description

2-methylthiooxazole is a chemical compound with the molecular formula C4H5NOS. It belongs to the oxazole class of compounds which are heterocyclic molecules containing an oxygen and nitrogen atom in a five-membered ring. The "2-methylthio" prefix indicates the presence of a methyl group and a sulfur atom attached to the oxazole ring at the 2-position. 2-methylthiooxazole is known for its versatile reactivity and is utilized in various organic synthesis reactions to create pharmaceutical compounds, agrochemicals, and other functional materials. 2-methylthiooxazole also demonstrates potential as an intermediate in the production of fragrances and flavoring compounds due to its sulfur-containing functional group. Overall, 2-methylthiooxazole is a valuable building block in the development of diverse chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 201017-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,0,1 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 201017-90:
(8*2)+(7*0)+(6*1)+(5*0)+(4*1)+(3*7)+(2*9)+(1*0)=65
65 % 10 = 5
So 201017-90-5 is a valid CAS Registry Number.

201017-90-5SDS

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 2-methylsulfanyl-1,3-oxazole

1.2 Other means of identification

Product number -
Other names Oxazole,2-(methylthio)

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:201017-90-5 SDS

201017-90-5Relevant articles and documents

Monosubstituted Oxazoles. 1. Synthesis of 5-Substituted Oxazoles by Directed Alkylation

Shafer, Cynthia M.,Molinski, Tadeusz F.

, p. 551 - 555 (1998)

A general method is presented for synthesis of 2-(methylthio)-5-substituted oxazoles 2. Deprotonation of the readily available 2-(methylthio)oxazole (1) with n-BuLi occurs smoothly in the presence of TMEDA and regiospecifically at C5. The organometallic 1a added rapidly to aldehydes and other electrophiles to provide 5-substituted-2-(methylthio)oxazoles in very good to excellent yields. Reductive removal of the MeS group gave the desired 5-monosubstituted oxazoles 3 in good yield.

Nickel-catalyzed synthesis of oxazoles via C-S activation

Lee, Kyoungsoo,Counceller, Carla M.,Stambuli, James P.

supporting information; experimental part, p. 1457 - 1559 (2009/08/08)

The synthesis of 2-substituted oxazoles is achieved via nickel-catalyzed cross-coupling reaction of 2-methylthio-oxazole and various organozinc reagents. An extension of this method is demonstrated with a chemoselective, one-pot synthesis of unsymmetrical

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