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Methanone, (4,5-dihydro-4,4-dimethyl-2-oxazolyl)phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60031-37-0

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60031-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60031-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,3 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60031-37:
(7*6)+(6*0)+(5*0)+(4*3)+(3*1)+(2*3)+(1*7)=70
70 % 10 = 0
So 60031-37-0 is a valid CAS Registry Number.

60031-37-0SDS

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 (4,4-dimethyl-5H-1,3-oxazol-2-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names Methanone,(4,5-dihydro-4,4-dimethyl-2-oxazolyl)phenyl

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:60031-37-0 SDS

60031-37-0Relevant academic research and scientific papers

Zincation of 4,4-dimethyloxazoline using TMPZnCl·LiCl. A new preparation of 2-aryloxazolines

Haas, Diana,Hofmayer, Maximilian S.,Bresser, Tomke,Knochel, Paul

supporting information, p. 6415 - 6417 (2015/04/14)

The metalation of 4,4-dimethyloxazoline using TMPZnCl·LiCl provides a stable 2-zincated oxazolinyl reagent which readily undergoes palladium-catalyzed Negishi cross-couplings allowing a new access to 2-aryloxazolines. Cu-mediated acylation and allylation reactions also proceed in good yields. This journal is

Terminal oxazolinyloxiranes: synthesis, reaction with amines and regioselective β-lithiation

Degennaro, Leonardo,Capriati, Vito,Carlucci, Claudia,Florio, Saverio,Luisi, Renzo,Nuzzo, Irene,Cuocci, Corrado

experimental part, p. 8745 - 8755 (2009/12/28)

The synthesis of terminal oxazolinyloxiranes, even in enantioenriched form, has been performed by Darzens-type reaction of lithiated chloroalkyloxazolines with benzotriazolylmethanol (BtCH2OH) or by chloromethylation of 2-acyl-2-oxazolines. The

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