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isopropyl 2-phenyl-4,5-dihydro-1,3-oxazole-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37592-54-4

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37592-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37592-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,9 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 37592-54:
(7*3)+(6*7)+(5*5)+(4*9)+(3*2)+(2*5)+(1*4)=144
144 % 10 = 4
So 37592-54-4 is a valid CAS Registry Number.

37592-54-4Relevant academic research and scientific papers

METHODS OF TREATMENT WITH DEUTERATED ANALOGS OF D-SERINE

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Paragraph 181-182, (2020/12/11)

This disclosure relates to deuterated D-serine, pharmaceutically acceptable salts thereof, analogs and prodrugs thereof, pharmaceutical compositions thereof, and methods of use.

DEUTERATED ANALOGS OF D-SERINE AND USES THEREOF

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Paragraph 326-327, (2020/12/11)

This disclosure relates to deuterated D-serine, pharmaceutically acceptable salts thereof, analogs and prodrugs thereof, pharmaceutical compositions thereof, and methods of use.

DEUTERATED ANALOGS OF D-SERINE AND USES THEREOF

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Paragraph 237-238, (2019/06/11)

This disclosure relates to deuterated D-serine, pharmaceutically acceptable salts thereof, analogs and prodrugs thereof, pharmaceutical compositions thereof, and methods of use.

Preparation of new 2,4-disubstituted oxazoles from N-acylaziridines

Eastwood, Frank W.,Perlmutter, Patrick,Yang, Qi

, p. 35 - 42 (2007/10/03)

The efficiency of the ring enlargement of 2-substituted N-acylaziridines to dihydrooxazoles followed by nickel peroxide oxidation to give 2,4-disubstituted oxazoles as a synthetic route is examined. Sodium iodide-promoted ring enlargements work well for N-acylaziridines bearing electron-donating 2-substituents. For N-acylaziridines bearing electron-withdrawing 2-substituents, the best results are obtained using acid-promoted rearrangement.

Preparation of new 2,4-disubstituted oxazoles

Eastwood,Perlmutter,Yang

, p. 2039 - 2042 (2007/10/02)

Ring enlargement of N-acylaziridines followed by nickel peroxide oxidation provides a variety of 2,4-disubstituted-1,3-oxazoles suitable for bis- and tris-oxazole synthesis.

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