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154136-90-0

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154136-90-0 Usage

General Description

2-(4-Methoxy-phenyl)-oxazole-4-carbaldehyde is a chemical compound with the molecular formula C11H9NO3. It belongs to the oxazole class of organic compounds. 2-(4-METHOXY-PHENYL)-OXAZOLE-4-CARBALDEHYDE is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is also used in the production of fluorescent dyes and as a reagent in organic chemistry reactions. The presence of a carbonyl group and a methoxyphenyl group in its structure makes 2-(4-Methoxy-phenyl)-oxazole-4-carbaldehyde a valuable intermediate in the synthesis of complex molecules with biological and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 154136-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,1,3 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 154136-90:
(8*1)+(7*5)+(6*4)+(5*1)+(4*3)+(3*6)+(2*9)+(1*0)=120
120 % 10 = 0
So 154136-90-0 is a valid CAS Registry Number.

154136-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)-1,3-oxazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-(4-Methoxyphenyl)oxazole-4-carbaldehyde

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:154136-90-0 SDS

154136-90-0Downstream Products

154136-90-0Relevant articles and documents

Thermal rearrangement of azido ketones into oxazoles via azirines: One-pot, metal-free heteroannulation to functionalized 1,3-oxazoles

Shah, Shailesh R.,Navathe, Sudhanva S.,Dikundwar, Amol G.,Guru Row, Tayur N.,Vasella, Andrea T.

supporting information, p. 264 - 267 (2013/02/26)

α-Azidoacetophenones were converted into 2-aryl-1,3-oxazole-4- carbaldehydes through rearrangement of the carbon framework upon exposure to DMF/POCl3. The unprecedented rearrangement occurs via alkenyl azides and 2H-azirines. A mechanism for this unusual reaction was proposed and evidenced.

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