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Ethanone, 1-[2-(4-methoxyphenyl)-5-methyl-4-oxazolyl]-, also known as 1-(2-(4-methoxyphenyl)-5-methyl-4-oxazolyl)ethanone, is a chemical compound with the molecular formula C12H13NO3. It is a derivative of ethanone (acetone) with a 4-oxazolyl group attached to the carbonyl carbon. The 4-oxazolyl group consists of a 4-methoxyphenyl ring and a 5-methyl group, which are connected to the oxazole ring. Ethanone, 1-[2-(4-methoxyphenyl)-5-methyl-4-oxazolyl]- is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those with potential applications in the treatment of neurological disorders and as herbicides. Its unique structure and properties make it a valuable compound for further research and development in the field of organic chemistry.

3222-92-2

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3222-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3222-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3222-92:
(6*3)+(5*2)+(4*2)+(3*2)+(2*9)+(1*2)=62
62 % 10 = 2
So 3222-92-2 is a valid CAS Registry Number.

3222-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(4-methoxyphenyl)-5-methyl-1,3-oxazol-4-yl]ethanone

1.2 Other means of identification

Product number -
Other names 4-Acetyl-2-<4-methoxy-phenyl>-5-methyl-oxazol

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:3222-92-2 SDS

3222-92-2Relevant academic research and scientific papers

Practical Deoxygenation of Oxazole N-Oxides by PCl 3/Collidine

Shirinian, Valerii Z.,Lonshakov, Ilya A.,Zakharov, Alexey V.,Lvov, Andrey G.,Krayushkin, Mikhail M.

, p. 414 - 420 (2019/01/10)

A new chemoselective method for the synthesis of 2-aryl-1,3-oxazoles by deoxygenation of the corresponding N-oxides has been developed. As the deoxygenation reagent, a previously unknown complex of collidine with phosphorus trichloride in a 2:1 ratio has

Synthesis and spectral properties of 3-(2-aryl-5-methyl-1,3-oxazol- 4-yl)-2-(2,5-dimethylthiophen-3-yl)cyclopent-2-en-1-ones

Lvov, Andrey G.,Shirinian, Valerii Z.,Kavun, Alexey M.,Krayushkin, Mikhail M.

supporting information, p. 277 - 279 (2015/01/16)

Alkylation of ethyl 4-(2,5-dimethylthiophen-3-yl)-3-oxobutanoate with 2-aryl-4-bromoacetyl-5-methyl-1,3-oxazole followed by decar-boxylation-cyclization of the intermediate diketo ester affords the title photochromic compounds. Relationship between the fl

Synthesis and photophysical studies of oxazole rings containing compounds as electron accepting units

Zhang, Caihong,Li, Lifeng,Wu, Hongjuan,Liu, Zhixun,Li, Junfen,Zhang, Guomei,Wen, Guangming,Shuang, Shaomin,Dong, Chuan,Choi, Martin M.F.

, p. 256 - 262 (2013/02/23)

A series of oxazole derivatives, 5-methyl-2-(p-methylphenyl)-4-acetyl oxazole (MMPAO), 5-methyl-2-(p-methoxyphenyl)-4-acetyl oxazole (MOPAO), 5-methyl-2-(p-N,N′-dimethylamino-phenyl)-4-acetyl oxazole (MDMAPAO) and 5-methyl-2-(p-N,N′-diphenylaminophenyl)-4

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