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90892-97-0

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90892-97-0 Usage

General Description

Ethanone, 1-(4-methyl-2-oxazolyl)- (9CI) is a chemical compound with the molecular formula C6H7NO2. It is also known by its chemical name 4-methyl-2-oxazolyl methyl ketone. Ethanone, 1-(4-methyl-2-oxazolyl)- (9CI) is a ketone derivative with an oxazole ring, and it is commonly used in the field of organic synthesis and pharmaceutical research. It is a yellow to brown liquid with a strong, pungent odor and is highly flammable. This chemical is known to be stable under normal temperatures and pressures, but it may decompose when exposed to extreme heat or light. It should be handled and stored with caution due to its flammability and potential reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 90892-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,9 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90892-97:
(7*9)+(6*0)+(5*8)+(4*9)+(3*2)+(2*9)+(1*7)=170
170 % 10 = 0
So 90892-97-0 is a valid CAS Registry Number.

90892-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Methyloxazol-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(4-Methyl-1,3-oxazol-2-yl)ethanone

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:90892-97-0 SDS

90892-97-0Downstream Products

90892-97-0Relevant articles and documents

Synthesis and Carbodemetalation Reactions of 4-Methyl- and 5-Aryl-2-(trimethylsilyl)oxazoles. C-C Bond Formation at C2 of the Oxazole Ring

Dondoni, Alessandro,Fantin, Giancarlo,Fogagnolo, Marco,Medici, Alessandro,Pedrini, Paola

, p. 3413 - 3420 (2007/10/02)

The title compounds 6a-d have been prepared by sequential lithiation and silylation of the corresponding 2-H oxazoles and isomerization of the resulting α-isocyano silyl enol ethers.Silyloxazoles 6a-d behave as stable 2-oxazolyl anion equivalents toward v

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