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5-phenyl-2H-1,3,4-oxadiazine-2,6(3H)-dione is a chemical compound with the molecular formula C9H6N2O3. It is a heterocyclic compound, specifically a derivative of 1,3,4-oxadiazine, which is a six-membered ring containing two nitrogen atoms and four oxygen atoms. The compound features a phenyl group (C6H5) attached to the 5-position of the oxadiazine ring, and it has two carbonyl groups (C=O) at the 2 and 6 positions. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is an important intermediate in organic chemistry, particularly in the development of new compounds with specific biological activities.

5335-46-6

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5335-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5335-46-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5335-46:
(6*5)+(5*3)+(4*3)+(3*5)+(2*4)+(1*6)=86
86 % 10 = 6
So 5335-46-6 is a valid CAS Registry Number.

5335-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyl-3H-1,3,4-oxadiazine-2,6-dione

1.2 Other means of identification

Product number -
Other names 5-Phenyl-3H-[1,3,4]oxadiazin-2,6-dion

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

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More Details:5335-46-6 SDS

5335-46-6Relevant academic research and scientific papers

SINTESI E CONFIGURAZIONE DI ACIDI α-IDRAZONOFENILACETICI

Monguzzi, R.,Scarpitta, G.,Ventura, P.,Pifferi, G.

, p. 394 - 404 (2007/10/02)

The synthesis of some α-hydrazonophenylacetic acids (II) by direct condensation of phenylglyoxylic acid with hydrazine or monosubstituted hydrazines and subsequent conversion into the α-alkoxycarbonylhydrazonophenylacetic acids (IV) according to three dif

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