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O-(2-nitrophenyl) dimethylcarbamothioate is a chemical compound with the molecular formula C9H10N2O4S. It is an organosulfur compound that features a 2-nitrophenyl group attached to a dimethylcarbamothioate moiety. O-(2-nitrophenyl) dimethylcarbamothioate is known for its potential use as an intermediate in the synthesis of various agrochemicals and pharmaceuticals, particularly in the production of insecticides and herbicides. Its structure includes a nitro group, which contributes to its reactivity and can be involved in reduction reactions, and a thiocarbonyl group, which is characteristic of carbamothioates and can participate in various chemical transformations. The compound's properties and reactivity make it a valuable building block in the development of new chemical entities with specific biological activities.

833-20-5

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833-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 833-20-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 833-20:
(5*8)+(4*3)+(3*3)+(2*2)+(1*0)=65
65 % 10 = 5
So 833-20-5 is a valid CAS Registry Number.

833-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name O-(2-nitrophenyl) N,N-dimethylcarbamothioate

1.2 Other means of identification

Product number -
Other names O-(2-nitrophenyl) dimethylcarbamothioate

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:833-20-5 SDS

833-20-5Relevant academic research and scientific papers

Microwave-mediated Newman-Kwart rearrangement in water

Hoffmann, Ina,Schatz, Jürgen

, p. 80692 - 80699 (2016/09/09)

For the first time the unimolecular Newman-Kwart rearrangement is performed in pure water. The elevated temperatures required for the 1,3-aryl shift are easily accomplished by microwave irradiation. Differently functionalized substrates underline the expe

A comparison of commercial microwave reactors for scale-up within process chemistry

Moseley, Jonathan D.,Lenden, Philip,Lockwood, Mark,Ruda, Katinka,Sherlock, Jon-Paul,Thomson, Anthony D.,Gilday, John P.

, p. 30 - 40 (2012/12/31)

Seven commercially available microwave reactors designed for limited scale-up have been investigated using a highly reliable and robust reaction (the Newman-Kwart rearrangement). The use of a single reaction has enabled the comparison to be made across the range of different reactor types and scales. Overall, all reactors gave reliable scale-up from small scale, and performance equivalent to one another on large scale. A more detailed comparison between them is given in the concluding section.

The Newman-Kwart rearrangement: A microwave kinetic study

Gilday, John P.,Lenden, Philip,Moseley, Jonathan D.,Cox, Brian G.

, p. 3130 - 3134 (2008/09/19)

(Chemical Equation Presented) The kinetic profile of the Newman-Kwart rearrangement has been evaluated using microwave heating. After first demonstrating equivalence between conventional convective heating and microwave heating, data was gathered and anal

The Newman-Kwart rearrangement re-evaluated by microwave synthesis

Moseley, Jonathan D.,Sankey, Rosalind F.,Tang, Olivier N.,Gilday, John P.

, p. 4685 - 4689 (2007/10/03)

The Newman-Kwart rearrangement (NKR) has been re-evaluated by microwave heating. Microwave technology has proven to be ideal for investigating this high temperature rearrangement and facilitated the confirmation of many aspects of this valuable reaction.

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