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2-(2-nitrophenyl)-5,6-dihydro-4H-1,3-oxazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90915-72-3

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90915-72-3 Usage

Type of compound

Heterocyclic compound

Constituent groups

Nitrophenyl group, oxazine ring

Usage

Building block for the synthesis of bioactive molecules in the pharmaceutical industry

Potential properties

Antibacterial and antifungal

Possible applications

Development of novel materials, reagent in organic chemistry reactions

Versatility

Wide range of potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 90915-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90915-72:
(7*9)+(6*0)+(5*9)+(4*1)+(3*5)+(2*7)+(1*2)=143
143 % 10 = 3
So 90915-72-3 is a valid CAS Registry Number.

90915-72-3Downstream Products

90915-72-3Relevant academic research and scientific papers

Microwave-Assisted Synthesis of 2-Aryl-2-oxazolines, 5,6-Dihydro-4H-1,3-oxazines, and 4,5,6,7-Tetrahydro-1,3-oxazepines

Mollo, María C.,Orelli, Liliana R.

supporting information, p. 6116 - 6119 (2016/12/09)

The first general procedure for the synthesis of 5- to 7-membered cyclic iminoethers by microwave-assisted cyclization of ω-amido alcohols promoted by polyphosphoric acid (PPA) esters is presented. 2-Aryl-2-oxazolines and 5,6-dihydro-4H-1,3-oxazines were efficiently prepared using ethyl polyphosphate/CHCl3. Trimethylsilyl polyphosphate in solvent-free conditions allowed for the synthesis of hitherto-unreported 4,5,6,7-tetrahydro-1,3-oxazepines. The method involves good to excellent yields and short reaction times.The reaction mechanism and the role of PPA esters were investigated in a chiral substrate.

Benzamide derivatives having a vasopressin antagonistic activity

-

, (2008/06/13)

This invention relates to new benzamide derivatives having a vasopressin antagonistic activity, etc. and represented by general formula (I): wherein R1is aryl optionally substituted with lower alkoxy, etc., R2is lower alkyl, etc., R3is hydrogen, etc., A is NH, etc., E is etc., X is —CH═CH—, —CH═N—, or S, and Y is a condensed heterocyclic group, etc., and pharmaceutically acceptable salts thereof, to processes for preparation thereof and to a pharmaceutical composition comprising the same.

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