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3-Phenyl-1,3-thiazinane-2,4-dione is a chemical compound with the molecular formula C10H8N2O2S. It is a derivative of the 1,3-thiazinane-2,4-dione class of compounds, characterized by the presence of a phenyl group attached to the 3-position of the heterocyclic ring. 3-phenyl-1,3-thiazinane-2,4-dione is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The presence of the phenyl group provides opportunities for further functionalization and modification, making it a versatile building block in organic chemistry. Its properties, such as solubility and stability, can be influenced by the specific substituents on the phenyl ring, which can be tailored for specific applications.

880-84-2

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880-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 880-84-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 880-84:
(5*8)+(4*8)+(3*0)+(2*8)+(1*4)=92
92 % 10 = 2
So 880-84-2 is a valid CAS Registry Number.

880-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-1,3-thiazinane-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-Phenyl-tetrahydro-1,3-thiazin-2,4-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:880-84-2 SDS

880-84-2Relevant academic research and scientific papers

Oxidation of thiourethanes, XII: Oxidative desulfuration of cyclic dithiocarbamates and -carbazates using hydrogen peroxide or hydrogen peroxide/sodium tungstate in a two-phase-system

Hanefeld,Schlitzer

, p. 413 - 415 (2007/10/02)

Cyclic dithiocarbamates and dithiocarbazates were desulfurized to the corresponding 2-oxo-analogues using H2O2 with or without addition of Na2WO4 in a two-phase-system.

1,3-Thiazines, XXXIII; oxidations of carbamothioates, VII: Oxidative desulfurisation of carbamodithioates by nitrous and nitric acid

Hanefeld,Gunes

, p. 521 - 527 (2007/10/02)

Carbamodithioates, mainly 2-thioxo-tetrahydro-4H-1,3-thiazine-4-ones 1, were converted to carbamothioates, mainly 5,6-dihydro-2H-1,3-thiazin-2,4(3H)-diones 2, by nitrous and nitric acid. With conc. nitric acid additional nitration of phenyl substituents was achieved.

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